P35354
Gene name |
PTGS2 |
Protein name |
Prostaglandin G/H synthase 2 |
Names |
Cyclooxygenase-2, COX-2, PHS II, Prostaglandin H2 synthase 2, PGH synthase 2, PGHS-2, Prostaglandin-endoperoxide synthase 2 |
Species |
Homo sapiens (Human) |
KEGG Pathway |
hsa:5743 |
EC number |
1.14.99.1: Miscellaneous |
Protein Class |
|
Descriptions
The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.
Autoinhibitory domains (AIDs)
Target domain |
|
Relief mechanism |
|
Assay |
cis-regPred |
Accessory elements
No accessory elements
Autoinhibited structure
Activated structure
8 structures for P35354
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| 5F19 | X-ray | 204 A | A/B | 19-569 | PDB |
| 5F1A | X-ray | 238 A | A/B | 19-570 | PDB |
| 5IKQ | X-ray | 241 A | A/B | 19-569 | PDB |
| 5IKR | X-ray | 234 A | A/B | 19-569 | PDB |
| 5IKT | X-ray | 245 A | A/B | 19-569 | PDB |
| 5IKV | X-ray | 251 A | A/B | 19-569 | PDB |
| 5KIR | X-ray | 270 A | A/B | 19-569 | PDB |
| AF-P35354-F1 | Predicted | AlphaFoldDB |
347 variants for P35354
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
|
rs533479217 CA34082403 |
3 | A>P | No |
ClinGen 1000Genomes TOPMed gnomAD |
|
|
CA344062794 rs533479217 |
3 | A>S | No |
ClinGen 1000Genomes TOPMed gnomAD |
|
|
rs200140544 CA34082402 |
4 | R>G | No |
ClinGen Ensembl |
|
|
rs779244806 CA1299772 |
5 | A>T | No |
ClinGen ExAC gnomAD |
|
|
CA344062780 rs1323381581 |
5 | A>V | No |
ClinGen TOPMed gnomAD |
|
| TCGA novel | 7 | L>M | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA344062743 rs755298351 |
12 | L>V | No |
ClinGen ExAC gnomAD |
|
|
CA34082399 rs200906212 |
13 | A>S | No |
ClinGen gnomAD |
|
|
rs1293553620 CA344062727 |
15 | S>G | No |
ClinGen gnomAD |
|
|
CA1299770 rs199946406 |
17 | T>A | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1157576579 CA344062707 |
18 | A>T | No |
ClinGen gnomAD |
|
| TCGA novel | 21 | C>F | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs199737603 CA1299758 |
23 | S>Y | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA344062636 rs1228524516 |
26 | C>Y | No |
ClinGen gnomAD |
|
|
CA344062613 rs771031623 |
29 | R>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs771031623 CA1299756 |
29 | R>Q | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA344062605 rs1394592753 |
31 | V>L | No |
ClinGen gnomAD |
|
|
CA34082303 rs201588411 |
32 | C>Y | No |
ClinGen Ensembl |
|
|
rs1571812529 CA344062591 |
33 | M>V | No |
ClinGen Ensembl |
|
|
rs1469636907 CA344062578 |
34 | S>R | No |
ClinGen TOPMed gnomAD |
|
|
rs746777440 CA1299755 |
34 | S>T | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA344062556 rs1467756337 |
38 | D>H | No |
ClinGen gnomAD |
|
|
CA1299754 rs777767886 |
40 | Y>C | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs777767886 CA344062538 |
40 | Y>F | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs945078063 CA34082302 |
40 | Y>H | No |
ClinGen Ensembl |
|
|
CA34082301 rs1039984985 |
43 | D>N | No |
ClinGen Ensembl |
|
|
COSM3376045 rs199661060 COSM3376044 CA34082299 |
46 | R>W | pancreas [Cosmic] | No |
ClinGen cosmic curated gnomAD |
|
rs1423245301 CA344062470 |
50 | Y>C | No |
ClinGen gnomAD |
|
|
CA344062430 rs1256555548 |
55 | S>L | No |
ClinGen gnomAD |
|
|
CA344062423 rs373745396 |
57 | P>A | No |
ClinGen ESP ExAC gnomAD |
|
|
CA1299721 rs764607381 |
57 | P>L | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA gnomAD |
|
CA344062408 rs764607381 |
57 | P>Q | No |
ClinGen ExAC gnomAD |
|
|
CA1299750 rs373745396 |
57 | P>S | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ESP ExAC NCI-TCGA gnomAD |
|
rs373745396 CA1299749 |
57 | P>T | No |
ClinGen ESP ExAC gnomAD |
|
|
COSM1689435 COSM1689434 rs1391277420 CA344062407 |
58 | E>K | skin [Cosmic] | No |
ClinGen cosmic curated gnomAD |
|
CA1299720 rs758723919 |
59 | F>L | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 62 | R>I | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA34082291 rs189809394 |
63 | I>L | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs189809394 CA1299719 |
63 | I>V | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
| TCGA novel | 64 | K>Q | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA344062364 rs1159681362 |
64 | K>T | No |
ClinGen gnomAD |
|
|
CA344062317 rs1558251045 |
71 | P>S | No |
ClinGen Ensembl |
|
|
rs764773998 CA1299718 |
73 | T>A | No |
ClinGen ExAC gnomAD |
|
|
CA1299717 rs759289241 |
74 | V>G | No |
ClinGen ExAC gnomAD |
|
|
CA344062295 rs1451690197 |
75 | H>N | No |
ClinGen TOPMed gnomAD |
|
|
rs753282331 CA1299716 |
75 | H>Q | No |
ClinGen ExAC gnomAD |
|
|
rs1195365633 CA344062278 |
77 | I>L | No |
ClinGen Ensembl |
|
|
rs1424440707 CA344062276 |
77 | I>T | No |
ClinGen gnomAD |
|
|
CA1299715 rs765917101 |
78 | L>F | No |
ClinGen ExAC gnomAD |
|
|
rs760272529 CA1299714 |
79 | T>S | No |
ClinGen ExAC gnomAD |
|
|
CA344062249 rs1229416920 |
81 | F>L | No |
ClinGen gnomAD |
|
|
rs866635655 CA34082290 |
83 | G>E | No |
ClinGen Ensembl |
|
|
CA344062239 rs1558250981 |
83 | G>R | No |
ClinGen Ensembl |
|
|
CA344062230 rs1305115452 |
84 | F>S | No |
ClinGen TOPMed |
|
|
CA344062216 rs1331433720 |
86 | N>D | No |
ClinGen gnomAD |
|
|
CA1299713 rs773231889 |
86 | N>K | No |
ClinGen ExAC TOPMed gnomAD |
|
| TCGA novel | 86 | N>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA1299712 rs772180278 |
87 | V>I | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
|
CA1299711 rs199619767 |
91 | I>L | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs1325689156 CA344062181 |
91 | I>T | No |
ClinGen gnomAD |
|
|
rs199619767 CA34082288 |
91 | I>V | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs1458352165 CA344062174 |
92 | P>L | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed gnomAD |
|
CA1299709 rs201046652 |
92 | P>T | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs200132172 COSM901217 COSM901218 CA1299708 |
95 | R>Q | Variant assessed as Somatic; 0.0 impact. large_intestine endometrium [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ExAC NCI-TCGA TOPMed gnomAD |
|
CA1299707 rs145215600 |
96 | N>S | No |
ClinGen ESP ExAC gnomAD |
|
| TCGA novel | 97 | A>T | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs747123567 CA1299705 |
98 | I>V | No |
ClinGen ExAC gnomAD |
|
|
rs1478192334 CA344062127 |
100 | S>G | No |
ClinGen gnomAD |
|
|
CA344062124 rs1378833561 |
100 | S>N | No |
ClinGen gnomAD |
|
|
CA344062077 rs1448517603 |
105 | S>Y | No |
ClinGen gnomAD |
|
|
CA344062074 rs1341821169 |
106 | R>G | No |
ClinGen gnomAD |
|
|
rs1428768336 CA344062053 |
109 | L>M | No |
ClinGen gnomAD |
|
| TCGA novel | 110 | I>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA1299678 rs749696563 |
112 | S>G | No |
ClinGen ExAC gnomAD |
|
|
CA344062024 rs1412293053 |
113 | P>T | No |
ClinGen gnomAD |
|
|
CA344062011 rs1451898767 |
115 | T>A | No |
ClinGen TOPMed |
|
|
CA1299677 rs377655174 |
115 | T>I | No |
ClinGen ESP ExAC gnomAD |
|
|
CA344061966 rs1571811749 |
121 | G>D | No |
ClinGen Ensembl |
|
|
rs200314986 CA1299676 |
122 | Y>* | No |
ClinGen ExAC gnomAD |
|
|
rs756733211 CA1299675 |
124 | S>I | No |
ClinGen ExAC gnomAD |
|
|
rs756733211 CA1299673 |
124 | S>N | No |
ClinGen ExAC gnomAD |
|
|
rs202013754 CA1299672 |
124 | S>R | No |
ClinGen ExAC gnomAD |
|
|
rs756733211 CA1299674 |
124 | S>T | No |
ClinGen ExAC gnomAD |
|
|
rs762779324 CA1299670 |
125 | W>L | No |
ClinGen ExAC |
|
|
rs763970406 CA1299671 |
125 | W>R | No |
ClinGen ExAC |
|
|
CA1299668 rs766574554 |
126 | E>G | No |
ClinGen ExAC |
|
|
CA1299669 rs775312199 |
126 | E>K | No |
ClinGen ExAC |
|
|
CA34082218 rs965556832 |
127 | A>G | No |
ClinGen Ensembl |
|
| TCGA novel | 128 | F>L | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs566984593 CA1299665 |
133 | Y>C | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA344061861 rs1319817234 |
137 | A>V | No |
ClinGen gnomAD |
|
| TCGA novel | 144 | D>A | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA1299662 rs536033236 |
146 | P>L | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
CA344061794 rs1239740288 |
147 | T>I | No |
ClinGen TOPMed |
|
|
rs780636784 CA1299660 |
148 | P>L | No |
ClinGen ExAC gnomAD |
|
|
CA1299646 rs774340680 |
154 | K>E | No |
ClinGen ExAC gnomAD |
|
|
CA344061740 rs1448238237 |
154 | K>R | No |
ClinGen TOPMed |
|
|
rs1308743303 CA344061728 |
156 | Q>K | No |
ClinGen gnomAD |
|
|
CA34082170 rs1057052111 |
157 | L>F | No |
ClinGen gnomAD |
|
|
CA344061719 rs1057052111 |
157 | L>V | No |
ClinGen gnomAD |
|
|
CA1299644 rs749747614 |
159 | D>G | No |
ClinGen ExAC gnomAD |
|
|
CA34082169 rs200842448 |
160 | S>A | No |
ClinGen gnomAD |
|
|
CA344061702 rs200842448 |
160 | S>P | No |
ClinGen gnomAD |
|
|
rs776157771 CA1299643 |
161 | N>S | No |
ClinGen ExAC gnomAD |
|
|
rs770236383 CA344061676 |
163 | I>M | No |
ClinGen ExAC gnomAD |
|
|
rs1455494038 CA344061645 |
168 | L>F | No |
ClinGen gnomAD |
|
|
rs199513587 CA34082168 |
172 | K>E | No |
ClinGen gnomAD |
|
|
CA1299639 rs770539837 |
172 | K>N | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 173 | F>L | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1393906666 CA344061611 |
173 | F>S | No |
ClinGen gnomAD |
|
|
rs1247457527 CA344061604 |
174 | I>S | No |
ClinGen TOPMed |
|
|
rs1285554656 CA344061581 |
177 | P>L | No |
ClinGen TOPMed |
|
|
rs1356667566 CA344061578 |
178 | Q>* | No |
ClinGen TOPMed |
|
|
rs535541309 CA34082167 |
178 | Q>R | No |
ClinGen TOPMed gnomAD |
|
|
CA344061527 rs1235898281 |
185 | A>S | No |
ClinGen gnomAD |
|
|
rs201493026 CA34082166 |
186 | F>L | No |
ClinGen TOPMed |
|
| TCGA novel | 186 | F>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 189 | Q>missing | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 192 | T>M | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs372267158 CA1299633 |
200 | H>Q | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
rs753612005 CA1299632 |
201 | K>M | No |
ClinGen ExAC gnomAD |
|
|
CA344061403 rs1440434396 |
201 | K>N | No |
ClinGen TOPMed |
|
|
CA344061402 rs1291036901 |
202 | R>* | No |
ClinGen gnomAD |
|
|
rs141500962 CA1299631 |
202 | R>Q | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
CA34082165 rs919237837 |
204 | P>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed |
|
CA344061366 rs1358824412 |
208 | N>D | No |
ClinGen gnomAD |
|
|
rs1388462023 CA344061357 |
209 | G>E | No |
ClinGen gnomAD |
|
|
rs751815873 CA344061359 CA1299629 |
209 | G>R | No |
ClinGen ExAC gnomAD |
|
|
rs1477645399 CA344061350 |
210 | L>R | No |
ClinGen TOPMed |
|
| TCGA novel | 216 | L>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA34082088 rs865832855 |
218 | H>Y | No |
ClinGen Ensembl |
|
|
CA344061276 rs1348890069 |
219 | I>M | No |
ClinGen gnomAD |
|
|
rs538414051 CA1299609 |
219 | I>V | No |
ClinGen 1000Genomes ExAC gnomAD |
|
|
rs765827639 CA1299607 |
221 | G>S | No |
ClinGen ExAC gnomAD |
|
|
rs558977656 CA1299606 |
224 | L>V | No |
ClinGen 1000Genomes ExAC gnomAD |
|
|
rs1281368683 CA344061230 |
227 | Q>E | No |
ClinGen TOPMed |
|
|
CA344061228 rs1291706641 |
227 | Q>L | No |
ClinGen gnomAD |
|
|
rs761122494 CA1299603 |
228 | R>C | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
|
VAR_016262 COSM424843 CA1299602 rs3218622 COSM424844 |
228 | R>H | breast [Cosmic] | No |
ClinGen cosmic curated UniProt 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
rs761122494 COSM1726628 CA1299604 COSM1726629 |
228 | R>S | liver [Cosmic] | No |
ClinGen cosmic curated ExAC TOPMed gnomAD |
|
COSM2123329 CA344061205 rs1194680056 COSM2123330 |
231 | R>C | Variant assessed as Somatic; 0.0 impact. pancreas [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated NCI-TCGA TOPMed |
|
rs1242261573 CA344061202 |
231 | R>L | No |
ClinGen TOPMed |
|
|
rs868858200 CA34082086 |
235 | D>N | No |
ClinGen Ensembl |
|
|
rs771747733 CA1299601 |
237 | K>R | No |
ClinGen ExAC gnomAD |
|
|
rs747632855 CA1299600 |
238 | M>V | No |
ClinGen ExAC TOPMed gnomAD |
|
| TCGA novel | 245 | G>A | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA344061088 rs1232662636 |
245 | G>E | No |
ClinGen TOPMed gnomAD |
|
|
CA344061093 rs1291537846 |
245 | G>R | No |
ClinGen TOPMed gnomAD |
|
|
CA344061086 rs1371551676 |
246 | E>Q | No |
ClinGen TOPMed gnomAD |
|
|
rs186230736 CA1299574 |
247 | M>I | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
CA1299573 rs745639034 |
248 | Y>H | No |
ClinGen ExAC gnomAD |
|
|
CA34082080 rs887880400 |
250 | P>L | No |
ClinGen TOPMed |
|
|
CA344061048 rs1318781700 |
251 | T>I | No |
ClinGen TOPMed gnomAD |
|
|
CA1299571 rs369291855 |
253 | K>R | No |
ClinGen ESP ExAC gnomAD |
|
|
CA344061030 rs1171417967 |
254 | D>V | No |
ClinGen TOPMed gnomAD |
|
|
CA344061021 rs1379502755 |
255 | T>I | No |
ClinGen TOPMed |
|
|
rs1422978070 CA344060968 |
263 | P>S | No |
ClinGen gnomAD |
|
|
CA1299569 rs779300029 |
264 | Q>H | No |
ClinGen ExAC gnomAD |
|
|
rs1274565158 CA344060937 |
267 | E>D | No |
ClinGen TOPMed |
|
|
CA1299566 rs756699181 |
270 | R>P | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA1299565 rs756699181 |
270 | R>Q | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs201723686 CA34082077 |
270 | R>W | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed gnomAD |
|
CA34082075 rs914524249 |
272 | A>S | No |
ClinGen Ensembl |
|
| TCGA novel | 275 | Q>* | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs767815237 CA1299563 |
275 | Q>R | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs763851146 CA1299560 |
285 | M>I | No |
ClinGen ExAC gnomAD |
|
|
rs755163066 CA34082073 |
286 | M>T | No |
ClinGen Ensembl |
|
|
rs775124209 CA1299558 |
290 | I>M | No |
ClinGen ExAC gnomAD |
|
|
rs762349072 CA1299559 |
290 | I>V | No |
ClinGen ExAC gnomAD |
|
|
CA1299557 rs769616622 |
291 | W>R | No |
ClinGen ExAC gnomAD |
|
|
CA1299554 rs148160346 |
293 | R>Q | No |
ClinGen ESP ExAC gnomAD |
|
|
COSM901212 COSM901211 rs776721278 CA344060777 |
293 | R>W | Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ExAC NCI-TCGA gnomAD |
|
CA1299552 rs200204426 COSM3803210 COSM3803211 |
300 | D>N | Variant assessed as Somatic; 0.0 impact. breast [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ExAC NCI-TCGA TOPMed gnomAD |
|
CA1299550 rs749311409 |
301 | V>M | No |
ClinGen ExAC gnomAD |
|
|
CA1299549 rs780245288 |
305 | E>D | No |
ClinGen ExAC gnomAD |
|
|
CA344060686 rs1215146515 |
306 | H>Y | No |
ClinGen gnomAD |
|
|
rs201228846 CA34082072 |
310 | G>D | No |
ClinGen TOPMed gnomAD |
|
|
rs1315583021 CA344060656 |
310 | G>R | No |
ClinGen gnomAD |
|
|
rs1228107146 CA344060583 |
320 | L>V | No |
ClinGen TOPMed gnomAD |
|
|
CA1299546 rs781689400 |
323 | I>L | No |
ClinGen ExAC gnomAD |
|
|
CA344060543 rs1444963388 |
324 | G>A | No |
ClinGen gnomAD |
|
| TCGA novel | 328 | K>N | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA1299525 rs199520386 |
328 | K>R | No |
ClinGen ExAC TOPMed gnomAD |
|
| TCGA novel | 328 | K>T | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1462305634 CA344060488 |
332 | E>A | No |
ClinGen gnomAD |
|
|
CA34082040 rs200843740 |
337 | H>R | No |
ClinGen Ensembl |
|
|
CA1299523 rs371762608 |
341 | Y>C | No |
ClinGen ESP ExAC gnomAD |
|
|
CA34082038 rs201764120 |
342 | H>Q | No |
ClinGen Ensembl |
|
|
CA344060405 rs1408773912 |
344 | K>Q | No |
ClinGen gnomAD |
|
|
rs764827141 CA1299522 COSM1601417 COSM1601416 |
349 | P>T | liver [Cosmic] | No |
ClinGen cosmic curated ExAC gnomAD |
|
rs1156433982 CA344060353 |
351 | L>Q | No |
ClinGen TOPMed |
|
|
rs759085374 CA1299521 |
355 | K>E | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1193969719 CA344060322 |
355 | K>N | No |
ClinGen gnomAD |
|
|
rs866862668 COSM3740875 COSM3740876 CA34082036 |
358 | Q>* | liver [Cosmic] | No |
ClinGen cosmic curated Ensembl |
|
CA344060293 rs1469641978 |
359 | Y>F | No |
ClinGen gnomAD |
|
| TCGA novel | 360 | Q>K | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs200479241 CA34082035 |
361 | N>S | No |
ClinGen TOPMed |
|
|
rs1443094098 CA344060274 |
362 | R>C | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed |
| TCGA novel | 367 | F>L | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs766401496 CA1299519 |
368 | N>S | No |
ClinGen ExAC gnomAD |
|
|
rs1285700548 CA344060220 |
370 | L>V | No |
ClinGen gnomAD |
|
|
rs1389494413 CA344060181 |
375 | P>S | No |
ClinGen TOPMed |
|
|
rs1369349606 CA344060155 |
379 | D>G | No |
ClinGen gnomAD |
|
|
rs767282746 CA1299516 |
382 | Q>H | No |
ClinGen ExAC gnomAD |
|
|
CA344060119 rs1373604934 |
384 | H>L | No |
ClinGen gnomAD |
|
|
CA344060120 rs1373604934 |
384 | H>R | No |
ClinGen gnomAD |
|
|
CA1299513 rs770054837 |
387 | K>E | No |
ClinGen ExAC gnomAD |
|
|
CA344060084 rs776759044 |
389 | N>D | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs776759044 CA1299511 |
389 | N>H | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA344060081 rs1412850897 |
389 | N>S | No |
ClinGen TOPMed gnomAD |
|
|
CA34082034 rs201708424 |
390 | Y>H | No |
ClinGen 1000Genomes gnomAD |
|
| TCGA novel | 393 | F>C | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA1299508 rs778162839 |
393 | F>L | No |
ClinGen ExAC gnomAD |
|
|
CA344060046 rs1456144285 |
394 | I>V | No |
ClinGen TOPMed gnomAD |
|
| TCGA novel | 395 | Y>C | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA34082033 rs748500299 |
399 | I>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA34082032 rs367650109 |
399 | I>T | No |
ClinGen ESP TOPMed gnomAD |
|
|
rs748500299 CA1299506 |
399 | I>V | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA1299504 rs5279 CA344059980 |
403 | H>Q | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
CA344059965 rs765917214 |
406 | T>A | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA1299502 rs765917214 |
406 | T>S | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA344059961 rs1163455221 |
407 | Q>K | No |
ClinGen TOPMed |
|
|
CA1299501 rs755696929 |
407 | Q>R | No |
ClinGen ExAC gnomAD |
|
|
CA34082031 rs202093833 |
408 | F>L | No |
ClinGen gnomAD |
|
|
rs750338422 CA344059923 |
412 | F>C | No |
ClinGen ExAC gnomAD |
|
|
CA1299500 rs750338422 |
412 | F>S | No |
ClinGen ExAC gnomAD |
|
|
rs1362856586 CA344059925 |
412 | F>V | No |
ClinGen gnomAD |
|
|
rs1413242782 CA344059912 |
414 | R>K | No |
ClinGen gnomAD |
|
|
CA344059895 rs1374896875 |
416 | I>T | No |
ClinGen gnomAD |
|
|
CA1299498 rs761649861 |
417 | A>T | No |
ClinGen ExAC gnomAD |
|
|
CA34082029 rs201373237 |
417 | A>V | No |
ClinGen Ensembl |
|
|
rs1388254963 CA344059885 |
418 | G>D | No |
ClinGen gnomAD |
|
|
rs773830437 CA34081971 |
420 | V>I | No |
ClinGen TOPMed gnomAD |
|
|
rs770221043 CA34081970 |
421 | A>T | No |
ClinGen TOPMed |
|
|
VAR_016263 rs4648279 CA1299480 |
428 | P>A | No |
ClinGen UniProt ExAC TOPMed dbSNP gnomAD |
|
|
rs984061797 CA34081969 |
428 | P>L | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed |
|
CA1299481 rs4648279 |
428 | P>S | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs4648279 CA344059814 |
428 | P>T | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs202020013 CA1299478 |
429 | A>S | No |
ClinGen ExAC gnomAD |
|
|
CA34081968 rs202020013 |
429 | A>T | No |
ClinGen ExAC gnomAD |
|
|
CA1299476 rs754018195 |
430 | V>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA344059796 rs1327334629 |
431 | Q>H | No |
ClinGen TOPMed |
|
|
CA1299474 rs760785915 |
432 | K>E | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 432 | K>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA344059787 rs1334024006 |
433 | V>I | No |
ClinGen TOPMed gnomAD |
|
|
CA344059768 rs1306444485 |
435 | Q>H | No |
ClinGen gnomAD |
|
|
rs139215497 CA34081967 |
436 | A>S | No |
ClinGen TOPMed gnomAD |
|
|
rs762156881 CA1299471 |
438 | I>T | No |
ClinGen ExAC gnomAD |
|
|
rs772624685 CA1299472 |
438 | I>V | No |
ClinGen ExAC gnomAD |
|
|
rs749712692 CA1299468 |
443 | Q>H | No |
ClinGen ExAC gnomAD |
|
|
rs769393500 CA1299466 |
449 | F>L | No |
ClinGen ExAC gnomAD |
|
|
rs745382650 CA1299465 |
454 | K>R | No |
ClinGen ExAC gnomAD |
|
|
CA1299464 rs780502264 |
455 | R>C | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 455 | R>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1274936592 CA344059612 |
457 | M>T | No |
ClinGen TOPMed |
|
|
rs1468314972 CA344059594 |
460 | P>A | No |
ClinGen gnomAD |
|
|
rs1032727927 CA34081963 |
463 | S>P | No |
ClinGen Ensembl |
|
|
CA34081962 rs998560580 |
466 | E>G | No |
ClinGen TOPMed gnomAD |
|
|
CA1299440 rs139787656 |
471 | K>E | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
CA34081889 rs777664238 |
471 | K>N | No |
ClinGen ExAC gnomAD |
|
|
CA1299438 rs758387677 |
474 | S>F | No |
ClinGen ExAC gnomAD |
|
|
CA1299437 rs752484376 |
475 | A>T | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA1299436 rs141702884 |
478 | E>K | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
CA1299435 rs754811569 |
479 | A>V | No |
ClinGen ExAC gnomAD |
|
|
CA1299433 rs767810225 |
481 | Y>C | No |
ClinGen ExAC gnomAD |
|
|
rs267598241 CA34081888 |
482 | G>S | No |
ClinGen Ensembl |
|
|
rs189679860 CA1299432 |
483 | D>N | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
CA1299431 rs751749337 |
484 | I>V | No |
ClinGen ExAC gnomAD |
|
|
CA1299430 rs764695479 |
487 | V>M | No |
ClinGen ExAC gnomAD |
|
|
rs5272 CA34081885 VAR_011980 |
488 | E>G | No |
ClinGen UniProt Ensembl dbSNP |
|
|
CA344059389 rs1210299227 |
489 | L>M | No |
ClinGen gnomAD |
|
| TCGA novel | 491 | P>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1338469357 CA344059338 |
497 | K>E | No |
ClinGen gnomAD |
|
|
COSM1287452 COSM1287451 CA1299428 rs776081537 |
497 | K>N | autonomic_ganglia [Cosmic] | No |
ClinGen cosmic curated ExAC TOPMed gnomAD |
|
rs1229095478 CA344059330 |
498 | P>S | No |
ClinGen gnomAD |
|
|
COSM531544 CA34081881 rs200408009 COSM531543 |
499 | R>L | lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] | No |
ClinGen cosmic curated 1000Genomes NCI-TCGA TOPMed gnomAD |
|
CA34081882 rs200408009 |
499 | R>Q | No |
ClinGen 1000Genomes TOPMed gnomAD |
|
|
COSM901205 CA1299427 rs201405348 COSM901206 |
499 | R>W | Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ExAC NCI-TCGA TOPMed gnomAD |
|
rs1444610498 CA344059317 |
501 | D>H | No |
ClinGen gnomAD |
|
|
rs1376804015 CA344059313 |
501 | D>V | No |
ClinGen gnomAD |
|
|
rs200926368 CA34081879 |
505 | G>S | No |
ClinGen Ensembl |
|
|
CA1299425 rs776118678 |
506 | E>D | No |
ClinGen ExAC gnomAD |
|
|
rs1558246298 CA344059275 |
507 | T>S | No |
ClinGen Ensembl |
|
|
CA1299424 rs770663212 |
508 | M>T | No |
ClinGen ExAC gnomAD |
|
|
rs200030471 CA34081878 |
510 | E>D | No |
ClinGen Ensembl |
|
|
rs5273 CA1299422 VAR_011981 |
511 | V>A | No |
ClinGen UniProt 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
|
rs5273 CA1299423 |
511 | V>G | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
rs771571521 CA1299421 |
517 | L>S | No |
ClinGen ExAC gnomAD |
|
|
CA344059194 rs1333546992 |
520 | L>F | No |
ClinGen gnomAD |
|
| TCGA novel | 522 | G>D | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA1299420 rs748021098 |
523 | N>K | No |
ClinGen ExAC gnomAD |
|
|
CA34081877 rs201342852 |
524 | V>I | No |
ClinGen ESP TOPMed gnomAD |
|
|
CA1299419 rs199820825 |
525 | I>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA344059160 rs199820825 |
525 | I>V | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1298886823 CA344059154 |
526 | C>R | No |
ClinGen TOPMed |
|
|
rs1202327911 CA344059140 |
528 | P>A | No |
ClinGen gnomAD |
|
|
CA344059139 rs1202327911 |
528 | P>S | No |
ClinGen gnomAD |
|
|
rs749145998 CA1299417 |
529 | A>T | No |
ClinGen ExAC gnomAD |
|
|
rs201922079 CA1299416 |
529 | A>V | No |
ClinGen ExAC gnomAD |
|
|
rs541453486 CA344059108 |
532 | K>N | No |
ClinGen TOPMed |
|
| TCGA novel | 532 | K>R | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA344059087 rs1332133558 |
535 | T>N | No |
ClinGen gnomAD |
|
|
CA344059053 rs1277787648 |
540 | V>G | No |
ClinGen TOPMed |
|
|
rs751835602 CA1299414 |
543 | Q>E | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA344059031 rs1356784766 |
544 | I>V | No |
ClinGen gnomAD |
|
|
rs200583134 CA1299412 |
545 | I>T | No |
ClinGen ExAC gnomAD |
|
|
rs895168815 CA34081875 |
546 | N>S | No |
ClinGen Ensembl |
|
|
rs1210271508 CA344059006 |
547 | T>I | No |
ClinGen TOPMed |
|
|
CA344058996 rs1392814387 |
549 | S>L | No |
ClinGen gnomAD |
|
| TCGA novel | 551 | Q>* | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 554 | I>F | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs765815931 CA1299410 |
554 | I>M | No |
ClinGen ExAC gnomAD |
|
|
CA1299409 rs759794443 |
556 | N>S | No |
ClinGen ExAC gnomAD |
|
|
CA344058941 rs1188212468 |
557 | N>S | No |
ClinGen TOPMed |
|
| TCGA novel | 558 | V>M | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1175587406 CA344058922 |
560 | G>R | No |
ClinGen gnomAD |
|
|
CA34081873 rs201730487 |
561 | C>S | No |
ClinGen Ensembl |
|
| TCGA novel | 562 | P>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA1299407 rs766007619 |
563 | F>L | No |
ClinGen ExAC gnomAD |
|
|
CA344058886 rs1171962882 |
565 | S>L | No |
ClinGen TOPMed |
|
|
CA34081871 rs201606460 |
567 | S>G | No |
ClinGen Ensembl |
|
|
CA34081870 rs924208743 |
569 | P>A | No |
ClinGen TOPMed gnomAD |
|
|
rs1213910146 CA344058860 |
569 | P>L | No |
ClinGen gnomAD |
|
|
rs924208743 CA344058863 |
569 | P>T | No |
ClinGen TOPMed gnomAD |
|
|
rs772864590 CA1299405 |
571 | P>A | No |
ClinGen ExAC gnomAD |
|
|
CA344058850 rs772864590 |
571 | P>S | No |
ClinGen ExAC gnomAD |
|
|
rs771520748 CA1299404 |
572 | E>D | No |
ClinGen ExAC gnomAD |
|
|
CA344058837 rs1281479804 |
573 | L>F | No |
ClinGen TOPMed gnomAD |
|
|
CA344058829 rs1350517032 |
574 | I>T | No |
ClinGen gnomAD |
|
|
CA344058808 rs1310616336 |
577 | V>A | No |
ClinGen TOPMed gnomAD |
|
|
rs774122358 CA1299402 |
578 | T>I | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs200492220 CA1299403 |
578 | T>P | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs933492734 CA34081869 |
579 | I>M | No |
ClinGen TOPMed gnomAD |
|
|
CA344058777 rs1370652272 |
582 | S>I | No |
ClinGen TOPMed |
|
|
CA1299401 rs768699687 |
585 | R>C | No |
ClinGen ExAC gnomAD |
|
|
COSM901197 COSM901198 rs749033694 CA1299400 |
585 | R>H | Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ExAC NCI-TCGA TOPMed gnomAD |
|
rs749033694 CA344058759 |
585 | R>P | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA1299398 rs201772944 |
586 | S>Y | No |
ClinGen ExAC TOPMed gnomAD |
|
|
COSM3689211 CA1299396 rs3218625 COSM3689210 VAR_016264 |
587 | G>R | large_intestine [Cosmic] | No |
ClinGen cosmic curated UniProt 1000Genomes ExAC TOPMed dbSNP gnomAD |
|
rs148865858 CA344058736 |
589 | D>E | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
CA1299392 rs755571974 |
590 | D>G | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA1299394 COSM3789250 COSM3789251 rs373482960 |
590 | D>N | Variant assessed as Somatic; 0.0 impact. urinary_tract [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ESP ExAC NCI-TCGA TOPMed gnomAD |
|
rs755571974 CA1299393 |
590 | D>V | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs754301528 CA1299391 |
591 | I>T | No |
ClinGen ExAC gnomAD |
|
|
rs201299558 COSM1222470 COSM1222471 CA34081866 |
600 | R>H | large_intestine [Cosmic] | No |
ClinGen cosmic curated ExAC gnomAD |
|
rs201299558 CA1299389 |
600 | R>L | No |
ClinGen ExAC gnomAD |
|
|
rs1558245968 CA344058672 |
600 | R>S | No |
ClinGen Ensembl |
No associated diseases with P35354
5 regional properties for P35354
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | DNA-directed DNA polymerase X | 185 - 574 | IPR002054 |
| domain | DNA polymerase beta-like, N-terminal domain | 188 - 254 | IPR010996 |
| binding_site | DNA polymerase family X, binding site | 356 - 375 | IPR019843 |
| domain | DNA polymerase beta, palm domain | 327 - 406 | IPR028207 |
| domain | DNA polymerase beta, thumb domain | 516 - 574 | IPR029398 |
Functions
| Description | ||
|---|---|---|
| EC Number | 1.14.99.1 | Miscellaneous |
| Subcellular Localization |
|
|
| PANTHER Family | ||
| PANTHER Subfamily | ||
| PANTHER Protein Class | ||
| PANTHER Pathway Category | No pathway information available | |
10 GO annotations of cellular component
| Name | Definition |
|---|---|
| caveola | A membrane raft that forms small pit, depression, or invagination that communicates with the outside of a cell and extends inward, indenting the cytoplasm and the cell membrane. Examples include flask-shaped invaginations of the plasma membrane in adipocytes associated with caveolin proteins, and minute pits or incuppings of the cell membrane formed during pinocytosis. Caveolae may be pinched off to form free vesicles within the cytoplasm. |
| cytoplasm | The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures. |
| endoplasmic reticulum | The irregular network of unit membranes, visible only by electron microscopy, that occurs in the cytoplasm of many eukaryotic cells. The membranes form a complex meshwork of tubular channels, which are often expanded into slitlike cavities called cisternae. The ER takes two forms, rough (or granular), with ribosomes adhering to the outer surface, and smooth (with no ribosomes attached). |
| endoplasmic reticulum lumen | The volume enclosed by the membranes of the endoplasmic reticulum. |
| endoplasmic reticulum membrane | The lipid bilayer surrounding the endoplasmic reticulum. |
| intracellular membrane-bounded organelle | Organized structure of distinctive morphology and function, bounded by a single or double lipid bilayer membrane and occurring within the cell. Includes the nucleus, mitochondria, plastids, vacuoles, and vesicles. Excludes the plasma membrane. |
| neuron projection | A prolongation or process extending from a nerve cell, e.g. an axon or dendrite. |
| nuclear inner membrane | The inner, i.e. lumen-facing, lipid bilayer of the nuclear envelope. |
| nuclear outer membrane | The outer, i.e. cytoplasm-facing, lipid bilayer of the nuclear envelope; continuous with the endoplasmic reticulum of the cell and sometimes studded with ribosomes. |
| protein-containing complex | A stable assembly of two or more macromolecules, i.e. proteins, nucleic acids, carbohydrates or lipids, in which at least one component is a protein and the constituent parts function together. |
7 GO annotations of molecular function
| Name | Definition |
|---|---|
| enzyme binding | Binding to an enzyme, a protein with catalytic activity. |
| heme binding | Binding to a heme, a compound composed of iron complexed in a porphyrin (tetrapyrrole) ring. |
| metal ion binding | Binding to a metal ion. |
| oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen | Catalysis of an oxidation-reduction (redox) reaction in which hydrogen or electrons are transferred from one donor, and two oxygen atoms is incorporated into a donor. |
| peroxidase activity | Catalysis of the reaction: a donor + a peroxide = an oxidized donor + 2 H2O. |
| prostaglandin-endoperoxide synthase activity | Catalysis of the reaction: arachidonate + donor-H2 + 2 O2 = prostaglandin H2 + acceptor + H2O. |
| protein homodimerization activity | Binding to an identical protein to form a homodimer. |
64 GO annotations of biological process
| Name | Definition |
|---|---|
| aging | A developmental process that is a deterioration and loss of function over time. Aging includes loss of functions such as resistance to disease, homeostasis, and fertility, as well as wear and tear. Aging includes cellular senescence, but is more inclusive. May precede death and may succeed developmental maturation (GO:0021700). |
| angiogenesis | Blood vessel formation when new vessels emerge from the proliferation of pre-existing blood vessels. |
| bone mineralization | The deposition of hydroxyapatite, a form of calcium phosphate with the formula Ca10(PO4)6(OH)2, in bone tissue. |
| brown fat cell differentiation | The process in which a relatively unspecialized cell acquires specialized features of a brown adipocyte, an animal connective tissue cell involved in adaptive thermogenesis. Brown adipocytes contain multiple small droplets of triglycerides and a high number of mitochondria. |
| cellular response to ATP | Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an ATP (adenosine 5'-triphosphate) stimulus. |
| cellular response to fluid shear stress | Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a fluid shear stress stimulus. Fluid shear stress is the force acting on an object in a system where the fluid is moving across a solid surface. |
| cellular response to heat | Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a heat stimulus, a temperature stimulus above the optimal temperature for that organism. |
| cellular response to hypoxia | Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus indicating lowered oxygen tension. Hypoxia, defined as a decline in O2 levels below normoxic levels of 20.8 - 20.95%, results in metabolic adaptation at both the cellular and organismal level. |
| cellular response to lead ion | Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a lead ion stimulus. |
| cellular response to mechanical stimulus | Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a mechanical stimulus. |
| cellular response to non-ionic osmotic stress | Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus indicating an increase or decrease in the concentration of non-ionic solutes (e.g. mannitol, sorbitol) in the environment. |
| cellular response to UV | Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an ultraviolet radiation (UV light) stimulus. Ultraviolet radiation is electromagnetic radiation with a wavelength in the range of 10 to 380 nanometers. |
| cyclooxygenase pathway | The chemical reactions and pathways by which prostaglandins are formed from arachidonic acid, and in which prostaglandin-endoperoxide synthase (cyclooxygenase) catalyzes the committed step in the conversion of arachidonic acid to the prostaglandin-endoperoxides PGG2 and PGH2. |
| decidualization | The cellular and vascular changes occurring in the endometrium of the pregnant uterus just after the onset of blastocyst implantation. This process involves the proliferation and differentiation of the fibroblast-like endometrial stromal cells into large, polyploid decidual cells that eventually form the maternal component of the placenta. |
| embryo implantation | Attachment of the blastocyst to the uterine lining. |
| hair cycle | The cyclical phases of growth (anagen), regression (catagen), quiescence (telogen), and shedding (exogen) in the life of a hair; one of the collection or mass of filaments growing from the skin of an animal, and forming a covering for a part of the head or for any part or the whole of the body. |
| inflammatory response | The immediate defensive reaction (by vertebrate tissue) to infection or injury caused by chemical or physical agents. The process is characterized by local vasodilation, extravasation of plasma into intercellular spaces and accumulation of white blood cells and macrophages. |
| learning | Any process in an organism in which a relatively long-lasting adaptive behavioral change occurs as the result of experience. |
| maintenance of blood-brain barrier | Maintaining the structure and function of the blood-brain barrier, thus ensuring specific regulated transport of substances (e.g. macromolecules, small molecules, ions) into the brain, and out of the brain into the blood circulation. |
| memory | The activities involved in the mental information processing system that receives (registers), modifies, stores, and retrieves informational stimuli. The main stages involved in the formation and retrieval of memory are encoding (processing of received information by acquisition), storage (building a permanent record of received information as a result of consolidation) and retrieval (calling back the stored information and use it in a suitable way to execute a given task). |
| negative regulation of calcium ion transport | Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of calcium ions into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. |
| negative regulation of cell cycle | Any process that stops, prevents or reduces the rate or extent of progression through the cell cycle. |
| negative regulation of cell population proliferation | Any process that stops, prevents or reduces the rate or extent of cell proliferation. |
| negative regulation of cysteine-type endopeptidase activity involved in apoptotic process | Any process that stops, prevents, or reduces the frequency, rate or extent of a cysteine-type endopeptidase activity involved in the apoptotic process. |
| negative regulation of intrinsic apoptotic signaling pathway in response to osmotic stress | Any process that stops, prevents or reduces the frequency, rate or extent of intrinsic apoptotic signaling pathway in response to osmotic stress. |
| negative regulation of smooth muscle contraction | Any process that stops, prevents, or reduces the frequency, rate or extent of smooth muscle contraction. |
| negative regulation of synaptic transmission, dopaminergic | Any process that stops, prevents, or reduces the frequency, rate or extent of dopaminergic synaptic transmission, the process of communication from a neuron to another neuron across a synapse using the neurotransmitter dopamine. |
| ovulation | The release of a mature ovum/oocyte from an ovary. |
| positive regulation of apoptotic process | Any process that activates or increases the frequency, rate or extent of cell death by apoptotic process. |
| positive regulation of brown fat cell differentiation | Any process that increases the rate, frequency, or extent of brown fat cell differentiation. Brown fat cell differentiation is the process in which a relatively unspecialized cell acquires specialized features of a brown adipocyte, an animal connective tissue cell involved in adaptive thermogenesis. Brown adipocytes contain multiple small droplets of triglycerides and a high number of mitochondria. |
| positive regulation of cell migration involved in sprouting angiogenesis | Any process that increases the frequency, rate or extent of cell migration involved in sprouting angiogenesis. Cell migration involved in sprouting angiogenesis is the orderly movement of endothelial cells into the extracellular matrix in order to form new blood vessels contributing to the process of sprouting angiogenesis. |
| positive regulation of fever generation | Any process that activates or increases the frequency, rate, or extent of fever generation. |
| positive regulation of fibroblast growth factor production | Any process that increases the rate, frequency or extent of the appearance of a fibroblast growth factor due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels. |
| positive regulation of nitric oxide biosynthetic process | Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of nitric oxide. |
| positive regulation of peptidyl-serine phosphorylation | Any process that activates or increases the frequency, rate or extent of the phosphorylation of peptidyl-serine. |
| positive regulation of platelet-derived growth factor production | Any process that increases the rate, frequency, or extent of the appearance of any platelet-derived growth factor due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels. |
| positive regulation of prostaglandin biosynthetic process | Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of prostaglandin. |
| positive regulation of protein import into nucleus | Any process that activates or increases the frequency, rate or extent of movement of proteins from the cytoplasm into the nucleus. |
| positive regulation of smooth muscle cell proliferation | Any process that activates or increases the rate or extent of smooth muscle cell proliferation. |
| positive regulation of smooth muscle contraction | Any process that activates or increases the frequency, rate or extent of smooth muscle contraction. |
| positive regulation of synaptic plasticity | A process that increases synaptic plasticity, the ability of synapses to change as circumstances require. They may alter function, such as increasing or decreasing their sensitivity, or they may increase or decrease in actual numbers. |
| positive regulation of synaptic transmission, glutamatergic | Any process that activates, maintains or increases the frequency, rate or extent of glutamatergic synaptic transmission, the process of communication from a neuron to another neuron across a synapse using the neurotransmitter glutamate. |
| positive regulation of transforming growth factor beta production | Any process that activates or increases the frequency, rate, or extent of production of transforming growth factor-beta. |
| positive regulation of vascular endothelial growth factor production | Any process that increases or activates the frequency, rate, or extent of production of vascular endothelial growth factor. |
| positive regulation of vasoconstriction | Any process that activates or increases the frequency, rate or extent of vasoconstriction. |
| prostaglandin biosynthetic process | The chemical reactions and pathways resulting in the formation of prostaglandins, any of a group of biologically active metabolites which contain a cyclopentane ring. |
| prostaglandin secretion | The regulated release of a prostaglandin, any of a group of biologically active metabolites which contain a cyclopentane ring, from a cell or a tissue. |
| regulation of blood pressure | Any process that modulates the force with which blood travels through the circulatory system. The process is controlled by a balance of processes that increase pressure and decrease pressure. |
| regulation of inflammatory response | Any process that modulates the frequency, rate or extent of the inflammatory response, the immediate defensive reaction (by vertebrate tissue) to infection or injury caused by chemical or physical agents. |
| regulation of neuroinflammatory response | Any process that modulates the frequency, rate or extent of neuroinflammatory response. |
| response to angiotensin | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an angiotensin stimulus. Angiotensin is any of three physiologically active peptides (angiotensin II, III, or IV) processed from angiotensinogen. |
| response to estradiol | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of stimulus by estradiol, a C18 steroid hormone hydroxylated at C3 and C17 that acts as a potent estrogen. |
| response to fatty acid | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a fatty acid stimulus. |
| response to fructose | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a fructose stimulus. |
| response to glucocorticoid | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a glucocorticoid stimulus. Glucocorticoids are hormonal C21 corticosteroids synthesized from cholesterol with the ability to bind with the cortisol receptor and trigger similar effects. Glucocorticoids act primarily on carbohydrate and protein metabolism, and have anti-inflammatory effects. |
| response to lipopolysaccharide | Any process that results in a change in state or activity of an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a lipopolysaccharide stimulus; lipopolysaccharide is a major component of the cell wall of gram-negative bacteria. |
| response to lithium ion | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a lithium (Li+) ion stimulus. |
| response to manganese ion | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a manganese ion stimulus. |
| response to nematode | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus from a nematode. |
| response to oxidative stress | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of oxidative stress, a state often resulting from exposure to high levels of reactive oxygen species, e.g. superoxide anions, hydrogen peroxide (H2O2), and hydroxyl radicals. |
| response to tumor necrosis factor | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a tumor necrosis factor stimulus. |
| response to vitamin D | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a vitamin D stimulus. |
| response to xenobiotic stimulus | Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus from a xenobiotic, a compound foreign to the organim exposed to it. It may be synthesized by another organism (like ampicilin) or it can be a synthetic chemical. |
| sensory perception of pain | The series of events required for an organism to receive a painful stimulus, convert it to a molecular signal, and recognize and characterize the signal. Pain is medically defined as the physical sensation of discomfort or distress caused by injury or illness, so can hence be described as a harmful stimulus which signals current (or impending) tissue damage. Pain may come from extremes of temperature, mechanical damage, electricity or from noxious chemical substances. This is a neurological process. |
7 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| O62664 | PTGS1 | Prostaglandin G/H synthase 1 | Bos taurus (Bovine) | PR |
| Q8HZR1 | PTGS1 | Prostaglandin G/H synthase 1 | Canis lupus familiaris (Dog) (Canis familiaris) | PR |
| Q9UPX0 | IGSF9B | Protein turtle homolog B | Homo sapiens (Human) | PR |
| P23219 | PTGS1 | Prostaglandin G/H synthase 1 | Homo sapiens (Human) | PR |
| P22437 | Ptgs1 | Prostaglandin G/H synthase 1 | Mus musculus (Mouse) | PR |
| Q05769 | Ptgs2 | Prostaglandin G/H synthase 2 | Mus musculus (Mouse) | PR |
| Q9C9U3 | DOX2 | Alpha-dioxygenase 2 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MLARALLLCA | VLALSHTANP | CCSHPCQNRG | VCMSVGFDQY | KCDCTRTGFY | GENCSTPEFL |
| 70 | 80 | 90 | 100 | 110 | 120 |
| TRIKLFLKPT | PNTVHYILTH | FKGFWNVVNN | IPFLRNAIMS | YVLTSRSHLI | DSPPTYNADY |
| 130 | 140 | 150 | 160 | 170 | 180 |
| GYKSWEAFSN | LSYYTRALPP | VPDDCPTPLG | VKGKKQLPDS | NEIVEKLLLR | RKFIPDPQGS |
| 190 | 200 | 210 | 220 | 230 | 240 |
| NMMFAFFAQH | FTHQFFKTDH | KRGPAFTNGL | GHGVDLNHIY | GETLARQRKL | RLFKDGKMKY |
| 250 | 260 | 270 | 280 | 290 | 300 |
| QIIDGEMYPP | TVKDTQAEMI | YPPQVPEHLR | FAVGQEVFGL | VPGLMMYATI | WLREHNRVCD |
| 310 | 320 | 330 | 340 | 350 | 360 |
| VLKQEHPEWG | DEQLFQTSRL | ILIGETIKIV | IEDYVQHLSG | YHFKLKFDPE | LLFNKQFQYQ |
| 370 | 380 | 390 | 400 | 410 | 420 |
| NRIAAEFNTL | YHWHPLLPDT | FQIHDQKYNY | QQFIYNNSIL | LEHGITQFVE | SFTRQIAGRV |
| 430 | 440 | 450 | 460 | 470 | 480 |
| AGGRNVPPAV | QKVSQASIDQ | SRQMKYQSFN | EYRKRFMLKP | YESFEELTGE | KEMSAELEAL |
| 490 | 500 | 510 | 520 | 530 | 540 |
| YGDIDAVELY | PALLVEKPRP | DAIFGETMVE | VGAPFSLKGL | MGNVICSPAY | WKPSTFGGEV |
| 550 | 560 | 570 | 580 | 590 | 600 |
| GFQIINTASI | QSLICNNVKG | CPFTSFSVPD | PELIKTVTIN | ASSSRSGLDD | INPTVLLKER |
| STEL |