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

7 structures for P16152

Entry ID Method Resolution Chain Position Source
1WMA X-ray 124 A A 2-277 PDB
2PFG X-ray 154 A A 2-277 PDB
3BHI X-ray 227 A A 2-277 PDB
3BHJ X-ray 177 A A 2-277 PDB
3BHM X-ray 180 A A 2-277 PDB
4Z3D X-ray 180 A A/B/C/D 2-277 PDB
AF-P16152-F1 Predicted AlphaFoldDB

263 variants for P16152

Variant ID(s) Position Change Description Diseaes Association Provenance
CA320272603
rs897824559
2 S>A No ClinGen
TOPMed
rs1441384240
CA409882182
3 S>C No ClinGen
gnomAD
CA409882178
rs1441384240
3 S>F No ClinGen
gnomAD
rs369228069
CA10015263
4 G>S No ClinGen
ExAC
gnomAD
rs371089618
CA10015264
5 I>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1223191674
CA409882239
6 H>D No ClinGen
TOPMed
gnomAD
rs1240399629
CA409882253
6 H>R No ClinGen
TOPMed
CA10015265
rs143215551
7 V>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs566688474
CA320272609
8 A>G No ClinGen
Ensembl
rs1318266119
CA409882276
8 A>S No ClinGen
gnomAD
rs745692534
CA10015266
9 L>P No ClinGen
ExAC
gnomAD
CA409882363
rs1429068762
11 T>I No ClinGen
TOPMed
gnomAD
TCGA novel 12 G>* Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1255330242
CA409882399
13 G>S No ClinGen
gnomAD
rs763746901
CA10015270
14 N>I No ClinGen
ExAC
gnomAD
CA320272624
rs1023456554
16 G>S No ClinGen
TOPMed
gnomAD
CA10015272
rs763329185
16 G>V No ClinGen
ExAC
TOPMed
gnomAD
CA10015273
rs766929443
18 G>S No ClinGen
ExAC
TOPMed
gnomAD
rs759895472
CA10015275
19 L>F No ClinGen
ExAC
gnomAD
CA10015274
rs751812271
19 L>V No ClinGen
ExAC
gnomAD
rs1327638590
CA409882571
19 L>W No ClinGen
gnomAD
CA409882613
rs1441381936
21 I>F No ClinGen
gnomAD
rs146570341
CA10015276
23 R>C No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA409882721
rs1374801279
23 R>H No ClinGen
gnomAD
rs752970795
CA409882763
24 D>H No ClinGen
ExAC
gnomAD
rs752970795
CA10015277
24 D>Y No ClinGen
ExAC
gnomAD
CA409882824
rs1272100463
25 L>V No ClinGen
gnomAD
rs1215228855
CA409882888
26 C>Y No ClinGen
gnomAD
CA409883006
rs1190579111
28 L>P No ClinGen
TOPMed
CA10015280
rs753977576
29 F>Y No ClinGen
ExAC
TOPMed
gnomAD
CA409883071
rs1471173349
30 S>L No ClinGen
gnomAD
CA10015282
rs757086930
31 G>V No ClinGen
ExAC
TOPMed
gnomAD
rs745656182
CA10015284
32 D>N No ClinGen
ExAC
gnomAD
CA10015286
rs779831065
37 A>T No ClinGen
ExAC
gnomAD
CA409883355
rs1356237695
37 A>V No ClinGen
gnomAD
rs775955102
CA10015289
38 R>Q No ClinGen
ExAC
gnomAD
rs768453981
CA10015288
38 R>W No ClinGen
ExAC
CA10015290
rs761398228
40 V>M No ClinGen
ExAC
TOPMed
gnomAD
CA409883589
rs1195611627
42 R>G No ClinGen
gnomAD
CA409883599
rs1286647577
42 R>Q No ClinGen
gnomAD
CA10015293
rs759878913
43 G>S No ClinGen
ExAC
TOPMed
gnomAD
rs767914019
CA10015294
45 A>E No ClinGen
ExAC
gnomAD
CA409883830
rs1475577154
46 A>V No ClinGen
gnomAD
rs200223739
CA10015295
47 V>I No ClinGen
ExAC
TOPMed
gnomAD
rs1371575719
CA409883904
48 Q>* No ClinGen
gnomAD
TCGA novel 48 Q>P Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs760841760
CA10015296
49 Q>R No ClinGen
ExAC
TOPMed
gnomAD
rs1421450227
CA409884041
51 Q>* No ClinGen
gnomAD
CA409884115
rs1432771382
52 A>V No ClinGen
TOPMed
gnomAD
rs367857649
CA10015299
53 E>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1315732436
CA409884219
54 G>D No ClinGen
gnomAD
CA10015300
rs778704295
54 G>S No ClinGen
ExAC
TOPMed
gnomAD
rs1325522379
CA409884245
55 L>P No ClinGen
gnomAD
TCGA novel 56 S>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA409884278
rs1418542265
56 S>N No ClinGen
TOPMed
rs758236840
CA10015302
57 P>L No ClinGen
ExAC
gnomAD
CA320272676
rs951888249
58 R>H No ClinGen
Ensembl
CA409884375
rs1280254619
59 F>C No ClinGen
gnomAD
CA409884361
rs1419813148
59 F>L No ClinGen
TOPMed
gnomAD
rs1419813148
CA409884364
59 F>V No ClinGen
TOPMed
gnomAD
rs779953785
CA10015303
60 H>P No ClinGen
ExAC
gnomAD
CA409884400
rs779953785
60 H>R No ClinGen
ExAC
gnomAD
rs1213148153
CA409884389
60 H>Y No ClinGen
gnomAD
CA409884450
rs1159873364
61 Q>E No ClinGen
gnomAD
CA409884503
rs41540715
61 Q>H No ClinGen
ExAC
TOPMed
gnomAD
rs746822383
CA10015304
61 Q>P No ClinGen
ExAC
gnomAD
rs1374578653
CA409884506
62 L>V No ClinGen
gnomAD
CA10015306
rs555028304
63 D>N No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs370920023
CA320272686
64 I>F No ClinGen
gnomAD
CA409884585
rs9979814
64 I>M No ClinGen
ExAC
TOPMed
gnomAD
CA320272684
rs370920023
64 I>V No ClinGen
gnomAD
rs769401188
CA10015309
65 D>E No ClinGen
ExAC
TOPMed
gnomAD
rs543800905
CA10015311
69 S>N No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
TCGA novel 69 S>P Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1349189945
CA409884841
71 R>H No ClinGen
gnomAD
rs775778302
CA409884856
72 A>P No ClinGen
ExAC
rs775778302
CA10015313
72 A>T No ClinGen
ExAC
CA409884888
rs1259025375
72 A>V No ClinGen
TOPMed
gnomAD
CA409884892
rs558896125
73 L>M No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA409884900
rs558896125
73 L>V No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs117272030
CA10015317
74 R>L No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10015318
rs559267091
75 D>N No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA409884985
rs1455517132
75 D>V No ClinGen
gnomAD
CA10015319
rs142778878
76 F>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 77 L>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA409885030
rs766432246
77 L>V No ClinGen
ExAC
gnomAD
TCGA novel 78 R>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA409885058
rs1467343109
78 R>G No ClinGen
Ensembl
CA409885065
rs1048322369
COSM3405382
78 R>H Variant assessed as Somatic; 0.0 impact. central_nervous_system [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
TOPMed
gnomAD
rs1048322369
CA320272706
78 R>L No ClinGen
TOPMed
gnomAD
CA10015323
rs754868460
79 K>R No ClinGen
ExAC
gnomAD
rs1305498936
CA409885156
81 Y>* No ClinGen
TOPMed
gnomAD
CA10015327
rs777221378
81 Y>C No ClinGen
ExAC
TOPMed
gnomAD
rs529825233
CA10015326
81 Y>D No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA10015330
rs151043730
82 G>A No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10015331
rs151043730
82 G>E No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs200695117
CA10015328
82 G>R No ClinGen
ExAC
TOPMed
gnomAD
CA10015329
rs200695117
82 G>W No ClinGen
ExAC
TOPMed
gnomAD
CA409885189
rs1439950229
83 G>V No ClinGen
TOPMed
CA409885231
rs1332918930
85 D>E No ClinGen
gnomAD
rs1003256032
CA320272721
85 D>V No ClinGen
TOPMed
CA409885246
rs1305707920
86 V>A No ClinGen
TOPMed
rs1213360369
CA409885253
87 L>Q No ClinGen
gnomAD
rs1213360369
CA409885257
87 L>R No ClinGen
gnomAD
CA320272723
VAR_059053
rs1143663
88 V>I reduced affinity for NADPH and reduced activity towards daunorubicin and prostaglandin E2 [UniProt] No ClinGen
UniProt
TOPMed
dbSNP
gnomAD
rs776688059
CA10015333
89 N>S No ClinGen
ExAC
gnomAD
rs762056579
CA10015334
90 N>K No ClinGen
ExAC
gnomAD
CA320272726
rs1030669258
90 N>S No ClinGen
TOPMed
CA320272729
rs1000335693
91 A>T No ClinGen
Ensembl
rs1296409952
CA409885351
91 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
rs773365505
CA10015337
92 G>A No ClinGen
ExAC
gnomAD
TCGA novel 92 G>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs773365505
CA10015336
92 G>V No ClinGen
ExAC
gnomAD
CA409885434
rs1474667551
94 A>P No ClinGen
TOPMed
gnomAD
CA409885430
rs1474667551
94 A>T No ClinGen
TOPMed
gnomAD
rs1395588502
CA409885471
95 F>L No ClinGen
TOPMed
gnomAD
CA10015340
rs754702330
96 K>N No ClinGen
ExAC
gnomAD
rs751602193
CA10015339
96 K>R No ClinGen
ExAC
gnomAD
CA409885513
rs767383110
97 V>F No ClinGen
ExAC
TOPMed
gnomAD
CA10015341
rs767383110
97 V>L No ClinGen
ExAC
TOPMed
gnomAD
rs141259214
CA10015373
98 A>V No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1170972649
CA409885748
COSM1030475
100 P>S endometrium [Cosmic] No ClinGen
cosmic curated
gnomAD
rs1393836095
CA409885896
105 I>S No ClinGen
gnomAD
CA10015374
rs778116397
107 A>V No ClinGen
ExAC
rs774437766
CA10015377
109 V>L No ClinGen
ExAC
TOPMed
gnomAD
rs200192508
CA409886075
110 T>M No ClinGen
ExAC
TOPMed
CA10015378
rs200192508
110 T>R No ClinGen
ExAC
TOPMed
CA409886108
rs1415376106
112 K>E No ClinGen
TOPMed
rs557204729
CA320272930
112 K>I No ClinGen
gnomAD
rs772044820
CA10015379
113 T>A No ClinGen
ExAC
gnomAD
CA409886174
rs1437037247
114 N>D No ClinGen
gnomAD
rs150365005
CA10015380
114 N>K Variant assessed as Somatic; 0.0001386 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
rs760444957
CA10015381
115 F>L No ClinGen
ExAC
gnomAD
CA10015382
rs763917846
116 F>I No ClinGen
ExAC
gnomAD
CA409886235
rs763917846
116 F>L No ClinGen
ExAC
gnomAD
rs753663954
CA10015383
116 F>S No ClinGen
ExAC
gnomAD
CA10015385
rs761407628
119 R>* No ClinGen
ExAC
gnomAD
rs759028268
CA320272942
119 R>Q No ClinGen
TOPMed
gnomAD
rs764885114
CA10015387
121 V>G No ClinGen
ExAC
gnomAD
CA10015388
rs375784875
122 C>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 123 T>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10015389
rs757911931
126 L>F No ClinGen
ExAC
TOPMed
gnomAD
rs781715120
CA10015390
129 I>T No ClinGen
ExAC
gnomAD
CA10015391
rs753192675
130 K>I No ClinGen
ExAC
TOPMed
gnomAD
rs1346053730
CA409886685
131 P>L No ClinGen
gnomAD
CA10015393
VAR_031706
rs41557318
131 P>S No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
CA409886701
rs1459050066
132 Q>* No ClinGen
gnomAD
CA320272954
rs747156853
133 G>R No ClinGen
Ensembl
rs1286291461
CA409892476
134 R>T No ClinGen
TOPMed
CA10015472
rs760237383
137 N>D No ClinGen
ExAC
gnomAD
CA320273330
rs1031038422
137 N>S No ClinGen
Ensembl
rs770198762
COSM478554
CA10015473
138 V>I kidney [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
rs770198762
CA409892576
138 V>L No ClinGen
ExAC
TOPMed
gnomAD
rs1173180839
CA409892629
140 S>G No ClinGen
gnomAD
rs763204071
CA10015475
141 I>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA10015474
rs773828531
141 I>V No ClinGen
ExAC
TOPMed
gnomAD
rs751952306
CA10015477
142 M>I No ClinGen
ExAC
rs766768951
CA10015476
142 M>V No ClinGen
ExAC
TOPMed
gnomAD
COSM1030477
CA10015479
rs370632546
144 V>I Variant assessed as Somatic; 0.0 impact. large_intestine endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
1000Genomes
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA409892748
rs752649052
145 R>S No ClinGen
ExAC
TOPMed
gnomAD
CA409892764
rs1389111479
146 A>D No ClinGen
gnomAD
CA409892759
rs199962768
146 A>P No ClinGen
1000Genomes
ExAC
gnomAD
CA10015481
rs199962768
146 A>T No ClinGen
1000Genomes
ExAC
gnomAD
rs763917680
CA10015482
147 L>V No ClinGen
ExAC
gnomAD
TCGA novel 149 S>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1568957942
CA409892935
151 S>N No ClinGen
Ensembl
CA10015486
rs757294585
152 P>L No ClinGen
ExAC
gnomAD
COSM1196207
rs1030203718
CA320273350
152 P>S lung [Cosmic] No ClinGen
cosmic curated
TOPMed
CA10015488
rs745672468
153 E>G No ClinGen
ExAC
TOPMed
gnomAD
CA10015489
rs758058719
154 L>M No ClinGen
ExAC
gnomAD
CA320273361
rs746489070
158 F>C No ClinGen
Ensembl
CA10015493
rs773560089
159 R>C No ClinGen
ExAC
TOPMed
gnomAD
COSM1030478
CA10015495
rs146559297
159 R>H Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
1000Genomes
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA10015494
rs146559297
159 R>L No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs774636988
CA10015497
166 E>D No ClinGen
ExAC
gnomAD
CA320273369
rs976993481
166 E>G No ClinGen
Ensembl
rs557925178
CA10015499
169 V>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs557925178
CA409893371
169 V>M No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA320273377
rs922499873
170 G>A No ClinGen
Ensembl
rs775837893
CA10015500
171 L>F No ClinGen
ExAC
gnomAD
CA10015501
rs760643033
172 M>V No ClinGen
ExAC
gnomAD
rs1046874551
CA320273386
174 K>R No ClinGen
Ensembl
rs764197380
CA10015502
175 F>L No ClinGen
ExAC
gnomAD
rs1458662102
CA409893453
175 F>S No ClinGen
TOPMed
gnomAD
CA409893461
rs1437133285
176 V>G No ClinGen
gnomAD
CA10015503
rs753889721
176 V>M No ClinGen
ExAC
gnomAD
rs757208303
CA10015504
178 D>N No ClinGen
ExAC
TOPMed
gnomAD
CA10015505
rs765270229
178 D>V No ClinGen
ExAC
TOPMed
gnomAD
CA409893483
rs1288650046
180 K>E No ClinGen
gnomAD
rs1318349126
CA409893495
181 K>R No ClinGen
gnomAD
rs533864137
CA10015509
182 G>E No ClinGen
1000Genomes
ExAC
gnomAD
rs555473871
CA320273401
183 V>L No ClinGen
1000Genomes
TOPMed
gnomAD
rs555473871
CA320273399
183 V>M No ClinGen
1000Genomes
TOPMed
gnomAD
CA10015511
rs780703439
187 E>G No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 188 G>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs763436504
CA320273407
189 W>* No ClinGen
Ensembl
CA409893625
rs1252861298
190 P>L No ClinGen
gnomAD
CA409893624
rs1252861298
190 P>R No ClinGen
gnomAD
CA409893653
rs1473712205
192 S>N No ClinGen
gnomAD
CA10015514
rs199906618
193 A>T No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1246144650
CA409893678
193 A>V No ClinGen
TOPMed
CA10015517
rs752113715
195 G>E No ClinGen
ExAC
gnomAD
rs146758729
CA10015516
RCV000894661
195 G>R No ClinGen
ClinVar
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
rs1601323647
CA409893727
196 V>G No ClinGen
Ensembl
rs1408734538
CA409893715
196 V>L No ClinGen
gnomAD
CA409893717
rs1408734538
196 V>M No ClinGen
gnomAD
rs201334038
CA10015518
197 T>M No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10015520
rs546119820
198 K>M No ClinGen
1000Genomes
ExAC
gnomAD
TCGA novel 199 I>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs765253793
CA10015522
201 V>I No ClinGen
ExAC
TOPMed
gnomAD
CA409893807
rs765253793
201 V>L No ClinGen
ExAC
TOPMed
gnomAD
rs762808256
CA10015524
203 V>F No ClinGen
ExAC
TOPMed
gnomAD
rs762808256
CA10015525
203 V>I Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA409893899
rs1340099289
206 R>K No ClinGen
gnomAD
CA409893940
rs1040147297
207 I>M No ClinGen
TOPMed
gnomAD
CA10015528
rs754600918
209 A>S No ClinGen
ExAC
gnomAD
CA10015527
rs754600918
209 A>T No ClinGen
ExAC
gnomAD
rs779368600
CA10015531
211 K>Q No ClinGen
ExAC
rs746336766
CA10015532
213 S>N No ClinGen
ExAC
gnomAD
rs772480635
CA10015533
217 K>R No ClinGen
ExAC
gnomAD
CA409894364
rs1388206717
218 G>E No ClinGen
gnomAD
rs1371878931
CA409894396
219 D>E No ClinGen
gnomAD
TCGA novel 219 D>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA409894373
rs1168612130
219 D>H No ClinGen
gnomAD
rs1429227352
CA409894400
220 K>E No ClinGen
TOPMed
rs1412397891
CA409894421
221 I>V No ClinGen
gnomAD
rs1286354289
CA409894582
227 C>S No ClinGen
gnomAD
CA10015537
rs374414411
229 G>A No ClinGen
ESP
ExAC
gnomAD
CA320273442
rs964388540
231 V>M No ClinGen
Ensembl
CA320273444
rs573227330
232 R>K No ClinGen
Ensembl
CA409894816
rs1275357410
233 T>I No ClinGen
gnomAD
rs762932134
CA10015541
235 M>T No ClinGen
ExAC
TOPMed
gnomAD
rs1189297937
CA409894883
235 M>V No ClinGen
TOPMed
CA320273450
rs867128163
236 A>V No ClinGen
gnomAD
rs754001791
CA320273454
238 P>R No ClinGen
Ensembl
rs1203728473
CA409895035
240 A>S No ClinGen
TOPMed
CA409895111
rs1448728879
244 P>S No ClinGen
gnomAD
CA409895125
rs1189215235
245 E>K No ClinGen
TOPMed
gnomAD
rs1476785218
CA409895153
246 E>* No ClinGen
gnomAD
rs1476785218
CA409895151
246 E>K No ClinGen
gnomAD
rs759316194
CA10015544
247 G>D No ClinGen
ExAC
TOPMed
gnomAD
rs141295222
CA10015545
248 A>T No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA10015546
rs752394402
248 A>V No ClinGen
ExAC
TOPMed
gnomAD
rs148205009
CA10015547
250 T>N No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 251 P>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs146879523
CA409895327
253 Y>C No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs146879523
CA10015549
253 Y>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA409895381
rs1231206647
255 A>V No ClinGen
gnomAD
CA10015551
rs780496525
256 L>P No ClinGen
ExAC
TOPMed
gnomAD
CA10015552
rs747389864
258 P>S Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA409895481
rs1464320802
260 D>V No ClinGen
gnomAD
CA10015554
rs781536281
261 A>T No ClinGen
ExAC
gnomAD
TCGA novel 262 E>* Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs143175086
CA320273484
262 E>D No ClinGen
1000Genomes
ESP
ExAC
gnomAD
rs748338970
CA10015555
262 E>V No ClinGen
ExAC
TOPMed
gnomAD
CA320273485
rs867646435
263 G>S No ClinGen
TOPMed
gnomAD
CA320273486
rs1046674820
267 Q>H No ClinGen
TOPMed
gnomAD
rs762942037
CA10015559
272 K>R No ClinGen
ExAC
gnomAD
rs770896302
CA10015560
274 V>I No ClinGen
ExAC
TOPMed
gnomAD
CA10015561
rs147519087
275 E>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA409895912
rs1321771130
276 Q>* No ClinGen
gnomAD
rs759352463
CA10015562
276 Q>R No ClinGen
ExAC
gnomAD
CA10015563
rs767338903
277 W>C No ClinGen
ExAC
TOPMed
gnomAD

No associated diseases with P16152

1 regional properties for P16152

Type Name Position InterPro Accession
conserved_site Short-chain dehydrogenase/reductase, conserved site 181 - 209 IPR020904

Functions

Description
EC Number 1.1.1.71 With NAD(+) or NADP(+) as acceptor
Subcellular Localization
  • Cytoplasm
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

3 GO annotations of cellular component

Name Definition
cytosol The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.
extracellular exosome A vesicle that is released into the extracellular region by fusion of the limiting endosomal membrane of a multivesicular body with the plasma membrane. Extracellular exosomes, also simply called exosomes, have a diameter of about 40-100 nm.
extracellular vesicle Any vesicle that is part of the extracellular region.

8 GO annotations of molecular function

Name Definition
15-hydroxyprostaglandin dehydrogenase (NADP+) activity Catalysis of the reaction: NADP(+) + prostaglandin E(1) = 15-dehydro-prostaglandin E1 + H(+) + NADPH.
15-hydroxyprostaglandin-D dehydrogenase (NADP+) activity Catalysis of the reaction: NADP+ + (5Z,13E)-(15S)-9-alpha,15-dihydroxy-11-oxoprosta-5,13-dienoate = NADPH + H+ + (5Z,13E)-9-alpha-hydroxy-11,15-dioxoprosta-5,13-dienoate.
alcohol dehydrogenase (NADP+) activity Catalysis of the reaction: an alcohol + NADP+ = an aldehyde + NADPH + H+.
carbonyl reductase (NADPH) activity Catalysis of the reaction: R-CHOH-R' + NADP+ = R-CO-R' + NADPH + H+.
oxidoreductase activity Catalysis of an oxidation-reduction (redox) reaction, a reversible chemical reaction in which the oxidation state of an atom or atoms within a molecule is altered. One substrate acts as a hydrogen or electron donor and becomes oxidized, while the other acts as hydrogen or electron acceptor and becomes reduced.
oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor Catalysis of an oxidation-reduction (redox) reaction in which NADH or NADPH acts as a hydrogen or electron donor and reduces a quinone or a similar acceptor molecule.
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor Catalysis of an oxidation-reduction (redox) reaction in which a CH-OH group acts as a hydrogen or electron donor and reduces NAD+ or NADP.
prostaglandin-E2 9-reductase activity Catalysis of the reaction: (5Z,13E)-(15S)-9-alpha,11-alpha,15-trihydroxyprosta-5,13-dienoate + NADP+ = (5Z,13E)-(15S)-11-alpha,15-dihydroxy-9-oxoprosta-5,13-dienoate + NADPH.

6 GO annotations of biological process

Name Definition
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.
epithelial cell differentiation The process in which a relatively unspecialized cell acquires specialized features of an epithelial cell, any of the cells making up an epithelium.
glucocorticoid metabolic process The chemical reactions and pathways involving glucocorticoids, hormonal C21 corticosteroids synthesized from cholesterol. Glucocorticoids act primarily on carbohydrate and protein metabolism, and have anti-inflammatory effects.
positive regulation of reactive oxygen species metabolic process Any process that activates or increases the frequency, rate or extent of reactive oxygen species metabolic process.
vitamin K metabolic process The chemical reactions and pathways involving any of the forms of vitamin K, quinone-derived vitamins which are involved in the synthesis of blood-clotting factors in mammals. Vitamin K substances share a methylated naphthoquinone ring structure and vary in the aliphatic side chains attached to the molecule.
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.

13 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
Q9VLU5 Wwox WW domain-containing oxidoreductase Drosophila melanogaster (Fruit fly) PR
A6NN90 C2orf81 Uncharacterized protein C2orf81 Homo sapiens (Human) PR
Q9HBH5 RDH14 Retinol dehydrogenase 14 Homo sapiens (Human) PR
Q9NZC7 WWOX WW domain-containing oxidoreductase Homo sapiens (Human) PR
O75828 CBR3 Carbonyl reductase [NADPH] 3 Homo sapiens (Human) PR
Q91WL8 Wwox WW domain-containing oxidoreductase Mus musculus (Mouse) PR
Q8CEE7 Rdh13 Retinol dehydrogenase 13 Mus musculus (Mouse) PR
Q9ERI6 Rdh14 Retinol dehydrogenase 14 Mus musculus (Mouse) PR
Q9DAQ4 Uncharacterized protein C2orf81 homolog Mus musculus (Mouse) PR
Q28960 CBR1 Carbonyl reductase [NADPH] 1 Sus scrofa (Pig) PR
Q6AXP4 Uncharacterized protein C2orf81 homolog Rattus norvegicus (Rat) PR
A2RVM0 TIC32 Short-chain dehydrogenase TIC 32, chloroplastic Arabidopsis thaliana (Mouse-ear cress) PR
Q803A8 wwox WW domain-containing oxidoreductase Danio rerio (Zebrafish) (Brachydanio rerio) PR
10 20 30 40 50 60
MSSGIHVALV TGGNKGIGLA IVRDLCRLFS GDVVLTARDV TRGQAAVQQL QAEGLSPRFH
70 80 90 100 110 120
QLDIDDLQSI RALRDFLRKE YGGLDVLVNN AGIAFKVADP TPFHIQAEVT MKTNFFGTRD
130 140 150 160 170 180
VCTELLPLIK PQGRVVNVSS IMSVRALKSC SPELQQKFRS ETITEEELVG LMNKFVEDTK
190 200 210 220 230 240
KGVHQKEGWP SSAYGVTKIG VTVLSRIHAR KLSEQRKGDK ILLNACCPGW VRTDMAGPKA
250 260 270
TKSPEEGAET PVYLALLPPD AEGPHGQFVS EKRVEQW