Q06520
Gene name |
SULT2A1 (HST, STD) |
Protein name |
Sulfotransferase 2A1 |
Names |
ST2A1, Bile salt sulfotransferase, Dehydroepiandrosterone sulfotransferase, DHEA-ST, DHEA-ST8, Hydroxysteroid Sulfotransferase, HST, ST2, SULT2A3 |
Species |
Homo sapiens (Human) |
KEGG Pathway |
hsa:6822 |
EC number |
2.8.2.2: Sulfotransferases |
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 Q06520
236 variants for Q06520
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
|
rs989081337 CA309239504 |
2 | S>L | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed |
|
CA406639168 rs989081337 |
2 | S>W | No |
ClinGen TOPMed |
|
|
CA9544970 rs750713459 |
4 | D>N | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA gnomAD |
|
rs750713459 CA9544971 |
4 | D>Y | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 6 | L>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1350928234 CA406639136 |
7 | W>* | No |
ClinGen gnomAD |
|
|
CA309239480 rs750182780 |
7 | W>* | No |
ClinGen Ensembl |
|
|
rs761884884 CA9544968 |
7 | W>G | No |
ClinGen ExAC gnomAD |
|
|
rs1444730798 CA406639114 |
10 | G>R | No |
ClinGen gnomAD |
|
|
CA406639115 rs1444730798 |
10 | G>S | No |
ClinGen gnomAD |
|
|
CA406639110 rs1387776793 |
10 | G>V | No |
ClinGen TOPMed |
|
|
CA309239471 rs914455729 |
14 | P>A | No |
ClinGen TOPMed gnomAD |
|
|
CA9544965 rs759574847 |
14 | P>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA406639087 rs914455729 |
14 | P>S | No |
ClinGen TOPMed gnomAD |
|
|
CA9544964 rs774254425 |
15 | T>N | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
|
rs151119240 CA9544963 |
16 | M>T | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
rs748882283 CA9544962 |
17 | G>D | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs777552791 CA9544961 |
19 | R>S | No |
ClinGen ExAC gnomAD |
|
|
rs955869493 CA309239463 |
19 | R>T | No |
ClinGen TOPMed |
|
|
rs181193745 CA309239460 |
21 | E>* | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
CA9544958 rs780703704 |
21 | E>D | No |
ClinGen ExAC gnomAD |
|
|
rs181193745 CA9544959 |
21 | E>K | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs1030604616 CA309239448 |
22 | T>I | No |
ClinGen TOPMed gnomAD |
|
|
CA406639018 rs1423173698 |
24 | R>K | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA gnomAD |
|
rs1600044384 CA406638988 |
26 | V>G | No |
ClinGen Ensembl |
|
|
COSM998822 CA9544954 rs781199635 |
27 | R>C | Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ExAC NCI-TCGA TOPMed gnomAD |
|
CA9544953 rs758864007 |
27 | R>H | No |
ClinGen ExAC gnomAD |
|
|
CA9544951 rs765438555 |
28 | D>G | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA406638974 rs1453723177 |
28 | D>N | No |
ClinGen TOPMed gnomAD |
|
|
rs11083907 CA406638932 CA406638935 |
30 | F>L | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
CA406638943 rs1600044355 |
30 | F>L | No |
ClinGen Ensembl |
|
|
CA309239422 rs17851828 |
30 | F>S | No |
ClinGen Ensembl |
|
|
CA406638931 rs1224724913 |
31 | V>M | No |
ClinGen gnomAD |
|
|
rs764307310 CA9544948 |
32 | I>T | No |
ClinGen ExAC gnomAD |
|
|
rs746681436 CA406638899 |
33 | R>M | No |
ClinGen gnomAD |
|
| TCGA novel | 33 | R>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs746681436 CA309239405 |
33 | R>T | No |
ClinGen gnomAD |
|
|
CA309239400 rs140689729 |
34 | D>N | No |
ClinGen ESP TOPMed |
|
|
CA9544947 rs759526164 |
36 | D>N | No |
ClinGen ExAC |
|
|
rs964465274 CA309239394 |
37 | V>I | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed gnomAD |
|
CA9544946 rs774491560 |
39 | I>T | No |
ClinGen ExAC TOPMed gnomAD |
|
| TCGA novel | 40 | L>M | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1026088302 CA309239392 |
40 | L>S | No |
ClinGen Ensembl |
|
|
rs762746830 CA9544944 |
41 | T>A | No |
ClinGen ExAC gnomAD |
|
|
rs1481416290 CA406638782 |
42 | Y>* | No |
ClinGen gnomAD |
|
|
rs1176871720 CA406638792 |
42 | Y>H | No |
ClinGen TOPMed gnomAD |
|
|
CA406638779 rs1417222490 |
43 | P>T | No |
ClinGen TOPMed gnomAD |
|
|
rs772897551 VAR_083881 CA9544943 |
44 | K>E | sulfating activity toward both DHEA and pregnenolone is completely abolished [UniProt] | No |
ClinGen UniProt ExAC dbSNP gnomAD |
|
CA406638762 rs1475428758 |
44 | K>T | No |
ClinGen TOPMed gnomAD |
|
|
rs749519618 CA9544913 |
48 | N>D | No |
ClinGen ExAC gnomAD |
|
|
rs144058411 CA9544912 |
50 | L>V | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
COSM164686 CA406638574 rs1385507037 |
52 | E>D | breast [Cosmic] | No |
ClinGen cosmic curated gnomAD |
|
CA309237925 rs972423172 |
57 | M>T | No |
ClinGen TOPMed |
|
|
CA309237920 rs373097856 |
58 | H>P | No |
ClinGen ESP TOPMed |
|
| TCGA novel | 59 | S>F | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1176987252 CA406638530 |
59 | S>P | No |
ClinGen gnomAD |
|
|
CA406638507 rs1367291244 |
62 | D>G | No |
ClinGen TOPMed |
|
| TCGA novel | 62 | D>M | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA9544908 rs11569681 VAR_052520 RCV000961665 |
63 | A>P | No |
ClinGen ClinVar UniProt 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
|
CA406638492 rs1254523842 |
64 | K>N | No |
ClinGen gnomAD |
|
|
rs1283088941 CA406638487 |
65 | W>* | No |
ClinGen TOPMed |
|
|
rs1220380467 CA406638480 |
66 | I>V | No |
ClinGen gnomAD |
|
|
rs1315342366 CA406638450 |
70 | P>R | No |
ClinGen gnomAD |
|
|
CA406638452 rs1247329786 |
70 | P>S | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA gnomAD |
|
CA9544906 rs765075147 |
72 | W>* | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1600041112 CA406638435 |
72 | W>C | No |
ClinGen Ensembl |
|
|
rs761528504 CA9544905 |
73 | E>G | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA9544904 rs62529832 |
74 | R>* | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen 1000Genomes ExAC NCI-TCGA gnomAD |
|
CA9544903 rs763687131 |
74 | R>Q | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
|
COSM712132 rs760347203 CA9544902 |
75 | S>* | lung [Cosmic] | No |
ClinGen cosmic curated ExAC gnomAD |
|
rs1600041069 CA406638423 |
75 | S>T | No |
ClinGen Ensembl |
|
|
CA9544901 VAR_083882 rs775030275 |
76 | P>T | decreases of the sulfotransferase activity toward DHEA; decreases of the sulfotransferase activity toward pregnenolone [UniProt] | No |
ClinGen UniProt ExAC dbSNP gnomAD |
|
CA406638410 rs1451267917 |
77 | W>* | No |
ClinGen gnomAD |
|
|
rs1173056628 CA406638406 |
77 | W>C | No |
ClinGen gnomAD |
|
|
CA9544900 rs369760395 |
79 | E>D | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
CA309237856 rs954976546 |
79 | E>Q | No |
ClinGen TOPMed |
|
|
rs555815288 CA9544899 |
82 | I>T | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
CA406638367 rs1414880298 |
83 | G>E | No |
ClinGen gnomAD |
|
|
CA406638370 rs1419998849 |
83 | G>R | No |
ClinGen gnomAD |
|
|
rs749616468 CA9544896 |
87 | L>F | No |
ClinGen ExAC gnomAD |
|
|
CA9544895 rs567166520 COSM998820 |
90 | T>M | endometrium [Cosmic] | No |
ClinGen cosmic curated 1000Genomes ExAC TOPMed gnomAD |
|
rs1260309562 CA406638307 |
92 | S>I | No |
ClinGen gnomAD |
|
|
CA406638302 rs1426455235 |
93 | P>T | No |
ClinGen gnomAD |
|
|
rs755073119 CA9544891 |
94 | R>C | No |
ClinGen ExAC gnomAD |
|
|
rs751662500 CA406638294 |
94 | R>H | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA406638293 rs751662500 |
94 | R>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA9544890 rs751662500 |
94 | R>P | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1390653175 CA406638284 |
96 | F>L | No |
ClinGen TOPMed |
|
|
rs757208013 CA9544888 |
96 | F>S | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1383819713 CA406638268 |
98 | S>C | No |
ClinGen gnomAD |
|
|
rs1449632879 CA406638262 |
99 | H>P | No |
ClinGen TOPMed |
|
|
rs760295858 CA406638257 |
100 | L>F | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1391358905 CA406638255 |
100 | L>P | No |
ClinGen gnomAD |
|
|
CA9544884 rs760295858 |
100 | L>V | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA406638247 rs1211204087 |
102 | I>V | No |
ClinGen Ensembl |
|
|
rs752348210 CA9544883 |
103 | Q>R | No |
ClinGen ExAC |
|
|
CA406638225 rs1485730753 |
105 | F>L | No |
ClinGen gnomAD |
|
|
CA9544881 rs758904710 |
107 | K>N | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs999268893 CA309237794 |
108 | S>F | No |
ClinGen TOPMed |
|
|
rs186827680 CA9544880 |
111 | S>G | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
rs377270215 CA309237782 |
111 | S>I | No |
ClinGen ESP TOPMed |
|
|
rs377270215 CA309237785 |
111 | S>N | No |
ClinGen ESP TOPMed |
|
|
rs1443036677 CA406638177 |
112 | S>T | No |
ClinGen TOPMed |
|
|
rs771516118 CA406638167 |
113 | K>N | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1201118715 CA406638170 |
113 | K>T | No |
ClinGen gnomAD |
|
|
rs1600040874 CA406638152 |
115 | K>N | No |
ClinGen Ensembl |
|
|
CA9544861 rs763534870 |
116 | V>M | No |
ClinGen ExAC gnomAD |
|
|
CA9544859 rs762023981 CA9544858 |
120 | M>I | No |
ClinGen ExAC gnomAD |
|
|
CA9544860 rs773917138 |
120 | M>T | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA406638065 rs1251384720 |
122 | N>S | No |
ClinGen gnomAD |
|
| TCGA novel | 124 | R>G | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 129 | S>Y | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA9544855 rs747295631 |
130 | G>A | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA9544856 rs375232202 |
130 | G>S | No |
ClinGen ESP ExAC gnomAD |
|
|
rs747295631 CA9544854 |
130 | G>V | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA9544852 rs780085343 |
132 | F>L | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 133 | F>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 134 | W>L | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs555280855 CA9544851 |
135 | K>E | No |
ClinGen 1000Genomes ExAC gnomAD |
|
| TCGA novel | 137 | M>I | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1396324408 CA406637857 |
138 | K>M | No |
ClinGen TOPMed gnomAD |
|
|
CA9544849 rs749217830 |
141 | K>E | No |
ClinGen ExAC |
|
|
CA9544847 rs756091684 |
143 | P>Q | No |
ClinGen ExAC gnomAD |
|
|
rs1568640174 CA406637793 |
143 | P>S | No |
ClinGen Ensembl |
|
|
rs1389092731 CA406637779 |
144 | K>N | No |
ClinGen TOPMed |
|
|
rs781073099 CA9544845 |
146 | W>* | No |
ClinGen ExAC gnomAD |
|
|
CA9544844 rs754560843 |
146 | W>* | No |
ClinGen ExAC gnomAD |
|
|
CA406637766 rs1462170807 |
146 | W>R | No |
ClinGen TOPMed |
|
|
VAR_083883 rs751309613 CA9544843 |
147 | E>K | decreases of the sulfotransferase activity toward DHEA; no effect on the sulfotransferase activity toward pregnenolone [UniProt] | No |
ClinGen UniProt ExAC TOPMed dbSNP gnomAD |
|
VAR_083884 rs368067020 CA9544842 |
148 | E>K | Variant assessed as Somatic; 0.0 impact. decreases of the sulfotransferase activity toward DHEA; decreases of the sulfotransferase activity toward pregnenolone [NCI-TCGA, UniProt] | No |
ClinGen UniProt ESP ExAC NCI-TCGA TOPMed dbSNP gnomAD |
|
rs1437176746 CA406637724 |
149 | Y>H | No |
ClinGen gnomAD |
|
|
CA406637702 rs1251093322 |
150 | F>C | No |
ClinGen gnomAD |
|
|
rs1206719395 CA406637699 |
150 | F>L | No |
ClinGen gnomAD |
|
|
CA406637670 rs1290365762 |
152 | W>C | No |
ClinGen gnomAD |
|
|
CA9544841 rs139437036 |
152 | W>G | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
rs202030683 CA9544840 |
153 | F>C | No |
ClinGen ExAC gnomAD |
|
|
CA406637665 rs1323415556 |
153 | F>L | No |
ClinGen TOPMed |
|
|
rs982751588 CA309237089 |
156 | G>A | No |
ClinGen Ensembl |
|
|
rs764839731 CA9544820 |
160 | Y>C | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA406637599 rs1389175056 |
160 | Y>H | No |
ClinGen gnomAD |
|
|
CA9544819 rs757683079 |
161 | G>W | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA9544818 rs754425624 |
163 | W>* | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA9544817 CA309235606 rs200731291 |
163 | W>C | No |
ClinGen 1000Genomes ExAC gnomAD |
|
|
COSM3720360 rs767819209 CA309235602 |
165 | D>N | haematopoietic_and_lymphoid_tissue [Cosmic] | No |
ClinGen cosmic curated Ensembl |
|
rs775847836 CA9544815 |
168 | H>R | No |
ClinGen ExAC gnomAD |
|
|
rs928731908 CA406637527 |
170 | W>* | No |
ClinGen gnomAD |
|
|
CA309235600 rs928731908 |
170 | W>C | No |
ClinGen gnomAD |
|
|
rs1269238469 CA406637519 |
171 | M>I | No |
ClinGen gnomAD |
|
|
CA9544814 rs767678575 |
172 | P>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1200431372 CA406637507 |
173 | M>I | No |
ClinGen TOPMed |
|
|
rs774264978 CA9544812 |
173 | M>R | No |
ClinGen ExAC gnomAD |
|
|
CA406637508 rs774264978 |
173 | M>T | No |
ClinGen ExAC gnomAD |
|
|
CA9544813 rs759786814 |
173 | M>V | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs771096303 CA9544811 |
175 | E>* | No |
ClinGen ExAC gnomAD |
|
|
rs748025835 CA9544810 |
175 | E>A | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA9544809 rs776701058 |
176 | E>K | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs147230706 CA9544808 |
177 | K>E | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
| TCGA novel | 181 | L>F | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA406637441 rs1467995597 |
183 | S>N | No |
ClinGen gnomAD |
|
|
rs544733723 CA309235575 |
184 | Y>H | No |
ClinGen gnomAD |
|
|
rs780023162 CA9544805 |
185 | E>K | No |
ClinGen ExAC gnomAD |
|
|
rs1600035311 CA406637411 |
187 | L>P | No |
ClinGen Ensembl |
|
|
CA309235568 rs969882784 |
188 | K>N | No |
ClinGen Ensembl |
|
|
rs1416845694 CA406637391 |
189 | Q>* | No |
ClinGen gnomAD |
|
|
rs888475801 CA309233737 |
192 | G>R | No |
ClinGen TOPMed |
|
|
CA9544786 rs775399658 |
194 | T>I | No |
ClinGen ExAC gnomAD |
|
|
CA406637025 rs775399658 |
194 | T>N | No |
ClinGen ExAC gnomAD |
|
|
rs1484531915 CA406637017 |
196 | E>K | No |
ClinGen gnomAD |
|
|
CA9544784 rs371975368 |
199 | C>S | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
CA406636980 rs1276841213 |
200 | Q>H | No |
ClinGen gnomAD |
|
|
CA9544782 rs770501427 |
203 | G>E | No |
ClinGen ExAC gnomAD |
|
|
rs748785131 CA9544781 |
204 | K>Q | No |
ClinGen ExAC gnomAD |
|
|
CA9544780 rs529798485 |
205 | T>K | No |
ClinGen ExAC TOPMed |
|
|
CA309233715 rs529798485 |
205 | T>M | No |
ClinGen ExAC TOPMed |
|
|
CA9544778 rs753252958 |
207 | E>A | No |
ClinGen ExAC |
|
|
CA9544776 rs147399625 |
208 | P>S | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
rs370526585 CA9544773 |
209 | E>K | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ESP ExAC NCI-TCGA TOPMed gnomAD |
|
CA406636830 rs1307382428 |
213 | L>* | No |
ClinGen gnomAD |
|
| TCGA novel | 215 | L>I | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA9544772 rs763112217 |
216 | K>E | No |
ClinGen ExAC gnomAD |
|
|
rs377180978 CA9544771 |
216 | K>N | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
CA406636780 rs1568637387 |
217 | N>H | No |
ClinGen Ensembl |
|
| TCGA novel | 217 | N>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1423607864 CA406636758 |
218 | S>N | No |
ClinGen gnomAD |
|
|
CA406636756 rs1423607864 |
218 | S>T | No |
ClinGen gnomAD |
|
|
CA406636745 rs1249352984 |
219 | S>P | No |
ClinGen TOPMed |
|
|
rs772139550 CA9544767 |
222 | S>N | No |
ClinGen ExAC gnomAD |
|
|
rs759315831 CA9544766 |
223 | M>L | No |
ClinGen ExAC gnomAD |
|
|
CA406636683 rs1254155846 |
225 | E>* | No |
ClinGen gnomAD |
|
|
CA9544765 rs774037082 |
226 | N>S | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs11569680 CA309233675 |
227 | K>* | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
rs11569680 CA9544763 RCV000879187 |
227 | K>E | No |
ClinGen ClinVar 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
|
rs11569680 CA9544764 |
227 | K>Q | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
CA9544762 rs772686936 |
228 | M>T | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA9544761 rs769353265 |
229 | S>F | No |
ClinGen ExAC gnomAD |
|
|
CA9544759 rs148329743 |
230 | N>I | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
rs148329743 CA9544760 |
230 | N>S | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
CA406636630 rs1173559793 |
230 | N>Y | No |
ClinGen TOPMed |
|
|
rs1352184597 CA406636592 |
233 | L>I | No |
ClinGen TOPMed gnomAD |
|
|
CA406636590 rs1352184597 |
233 | L>V | No |
ClinGen TOPMed gnomAD |
|
|
rs747352904 CA9544757 |
235 | S>G | No |
ClinGen ExAC gnomAD |
|
|
rs1392182520 CA406636567 |
235 | S>N | No |
ClinGen TOPMed |
|
|
CA9544756 rs780320337 |
239 | V>L | No |
ClinGen ExAC gnomAD |
|
|
CA406636478 rs1368495524 |
241 | D>E | No |
ClinGen TOPMed |
|
|
CA406636444 rs750664796 |
244 | Q>P | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA9544754 rs750664796 |
244 | Q>R | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs190776413 CA9544753 |
245 | L>F | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs757338859 VAR_083885 CA9544752 |
246 | L>P | decreases of the sulfotransferase activity toward DHEA; decreases of the sulfotransferase activity toward pregnenolone [UniProt] | No |
ClinGen UniProt ExAC dbSNP gnomAD |
|
CA309233650 rs912944182 |
247 | R>T | No |
ClinGen TOPMed |
|
|
CA309233648 rs947041469 |
249 | G>S | No |
ClinGen TOPMed |
|
|
CA9544737 rs758752472 |
250 | V>A | No |
ClinGen ExAC gnomAD |
|
|
rs1426974048 CA406636311 |
252 | G>R | No |
ClinGen gnomAD |
|
|
rs1189011400 CA406636264 |
254 | W>* | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA gnomAD |
|
CA406636274 rs1186426230 |
254 | W>* | No |
ClinGen TOPMed |
|
|
CA309232219 rs866659042 |
255 | K>R | No |
ClinGen Ensembl |
|
|
rs1466120788 CA406636238 |
256 | N>S | No |
ClinGen gnomAD |
|
|
CA9544734 VAR_083886 rs779218418 |
258 | F>L | decreases of the sulfotransferase activity toward DHEA; decreases of the sulfotransferase activity toward pregnenolone [UniProt] | No |
ClinGen UniProt ExAC dbSNP gnomAD |
|
VAR_083886 CA9544735 rs746239667 |
258 | F>L | decreases of the sulfotransferase activity toward DHEA; decreases of the sulfotransferase activity toward pregnenolone [UniProt] | No |
ClinGen UniProt ExAC dbSNP gnomAD |
|
VAR_052521 CA9544733 rs11569679 |
261 | A>T | No |
ClinGen UniProt 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
|
rs753928755 VAR_083887 CA9544732 |
262 | Q>E | decreases of the sulfotransferase activity toward DHEA; no effect on the sulfotransferase activity toward pregnenolone [UniProt] | No |
ClinGen UniProt ExAC dbSNP gnomAD |
|
CA309232212 rs753928755 |
262 | Q>K | No |
ClinGen ExAC gnomAD |
|
|
CA9544731 rs764311389 |
263 | A>G | No |
ClinGen ExAC gnomAD |
|
|
rs754922906 CA9544730 |
264 | E>A | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1568636259 CA406636120 |
265 | D>N | No |
ClinGen Ensembl |
|
|
CA9544728 rs751509523 COSM1525576 |
269 | L>F | lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] | No |
ClinGen cosmic curated ExAC NCI-TCGA gnomAD |
|
rs750526898 CA309232202 |
270 | F>S | No |
ClinGen Ensembl |
|
|
rs1225285029 CA406636022 |
274 | M>I | No |
ClinGen Ensembl |
|
|
CA406636026 rs766193413 |
274 | M>K | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA9544727 rs766193413 |
274 | M>T | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA406636029 rs1395957589 |
274 | M>V | No |
ClinGen gnomAD |
|
| TCGA novel | 277 | L>R | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA309232199 rs1032191564 |
278 | P>S | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed gnomAD |
|
rs149563641 CA9544726 |
279 | R>Q | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
CA9544724 rs764823849 |
283 | P>S | No |
ClinGen ExAC gnomAD |
|
|
rs1442952150 CA406635869 COSM3797331 CA406635868 |
284 | W>R | Variant assessed as Somatic; 0.0 impact. urinary_tract [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated NCI-TCGA gnomAD |
|
CA309232183 rs1013330593 |
285 | E>D | No |
ClinGen Ensembl |
No associated diseases with Q06520
1 regional properties for Q06520
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | Sulfotransferase domain | 34 - 277 | IPR000863 |
Functions
| Description | ||
|---|---|---|
| EC Number | 2.8.2.2 | Sulfotransferases |
| Subcellular Localization |
|
|
| PANTHER Family | ||
| PANTHER Subfamily | ||
| PANTHER Protein Class | ||
| PANTHER Pathway Category | No pathway information available | |
2 GO annotations of cellular component
5 GO annotations of molecular function
| Name | Definition |
|---|---|
| 3'-phosphoadenosine 5'-phosphosulfate binding | Binding to 3'-phosphoadenosine 5'-phosphosulfate (PAPS), a naturally occurring mixed anhydride. It is an intermediate in the formation of a variety of sulfo compounds in biological systems. |
| alcohol sulfotransferase activity | Catalysis of the reaction: 3'-phosphoadenosine 5'-phosphosulfate + an alcohol = adenosine 3',5'-bisphosphate + an alkyl sulfate. |
| bile-salt sulfotransferase activity | Catalysis of the reaction: 3'-phosphoadenosine 5'-phosphosulfate + taurolithocholate = adenosine 3',5'-bisphosphate + taurolithocholate sulfate. |
| steroid sulfotransferase activity | Catalysis of the reaction: 3'-phosphoadenosine 5'-phosphosulfate + a phenolic steroid = adenosine 3',5'-bisphosphate + steroid O-sulfate. |
| sulfotransferase activity | Catalysis of the transfer of a sulfate group from 3'-phosphoadenosine 5'-phosphosulfate to the hydroxyl group of an acceptor, producing the sulfated derivative and 3'-phosphoadenosine 5'-phosphate. |
9 GO annotations of biological process
| Name | Definition |
|---|---|
| 3'-phosphoadenosine 5'-phosphosulfate metabolic process | The chemical reactions and pathways involving 3'-phosphoadenosine 5'-phosphosulfate, a naturally occurring mixed anhydride. It is an intermediate in the formation of a variety of sulfo compounds in biological systems. |
| bile acid catabolic process | The chemical reactions and pathways resulting in the breakdown of bile acids, any of a group of steroid carboxylic acids occurring in bile. |
| cholesterol metabolic process | The chemical reactions and pathways involving cholesterol, cholest-5-en-3 beta-ol, the principal sterol of vertebrates and the precursor of many steroids, including bile acids and steroid hormones. It is a component of the plasma membrane lipid bilayer and of plasma lipoproteins and can be found in all animal tissues. |
| ethanol catabolic process | The chemical reactions and pathways resulting in the breakdown of ethanol, CH3-CH2-OH, a colorless, water-miscible, flammable liquid produced by alcoholic fermentation. |
| lipid catabolic process | The chemical reactions and pathways resulting in the breakdown of lipids, compounds soluble in an organic solvent but not, or sparingly, in an aqueous solvent. |
| steroid metabolic process | The chemical reactions and pathways involving steroids, compounds with a 1,2,cyclopentanoperhydrophenanthrene nucleus. |
| sulfation | The addition of a sulfate group to a molecule. |
| thyroid hormone metabolic process | The chemical reactions and pathways involving any of the compounds secreted by the thyroid gland, largely thyroxine and triiodothyronine. |
| xenobiotic metabolic process | The chemical reactions and pathways involving a xenobiotic compound, 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. |
11 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| P19217 | SULT1E1 | Sulfotransferase 1E1 | Bos taurus (Bovine) | PR |
| P49888 | SULT1E1 | Sulfotransferase 1E1 | Homo sapiens (Human) | PR |
| Q9BR01 | SULT4A1 | Sulfotransferase 4A1 | Homo sapiens (Human) | PR |
| P49891 | Sult1e1 | Sulfotransferase 1E1 | Mus musculus (Mouse) | PR |
| O35403 | Sult3a1 | Amine sulfotransferase | Mus musculus (Mouse) | PR |
| Q3UZZ6 | Sult1d1 | Sulfotransferase 1 family member D1 | Mus musculus (Mouse) | PR |
| P0CC03 | Sult6b1 | Sulfotransferase 6B1 | Mus musculus (Mouse) | PR |
| P49890 | Ste2 | Estrogen sulfotransferase Ste2 | Rattus norvegicus (Rat) | PR |
| P17988 | Sult1a1 | Sulfotransferase 1A1 | Rattus norvegicus (Rat) | PR |
| Q9FX55 | STO9 | Cytosolic sulfotransferase 9 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| Q9STQ6 | SOT3 | Cytosolic sulfotransferase 3 | Arabidopsis thaliana (Mouse-ear cress) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MSDDFLWFEG | IAFPTMGFRS | ETLRKVRDEF | VIRDEDVIIL | TYPKSGTNWL | AEILCLMHSK |
| 70 | 80 | 90 | 100 | 110 | 120 |
| GDAKWIQSVP | IWERSPWVES | EIGYTALSET | ESPRLFSSHL | PIQLFPKSFF | SSKAKVIYLM |
| 130 | 140 | 150 | 160 | 170 | 180 |
| RNPRDVLVSG | YFFWKNMKFI | KKPKSWEEYF | EWFCQGTVLY | GSWFDHIHGW | MPMREEKNFL |
| 190 | 200 | 210 | 220 | 230 | 240 |
| LLSYEELKQD | TGRTIEKICQ | FLGKTLEPEE | LNLILKNSSF | QSMKENKMSN | YSLLSVDYVV |
| 250 | 260 | 270 | 280 | ||
| DKAQLLRKGV | SGDWKNHFTV | AQAEDFDKLF | QEKMADLPRE | LFPWE |