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

1 structures for Q13585

Entry ID Method Resolution Chain Position Source
AF-Q13585-F1 Predicted AlphaFoldDB

450 variants for Q13585

Variant ID(s) Position Change Description Diseaes Association Provenance
CA415266263
rs1317478046
3 P>S No ClinGen
gnomAD
rs1215653895
CA415266275
5 L>V No ClinGen
gnomAD
rs1157091999
CA415266284
6 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
rs781043035
CA10540172
7 V>F No ClinGen
ExAC
gnomAD
CA10540173
rs201148153
10 P>T No ClinGen
1000Genomes
ExAC
gnomAD
CA10540175
rs779004211
11 Y>C No ClinGen
ExAC
gnomAD
rs1412998291 11 Y>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs748396836
CA10540176
12 G>D No ClinGen
ExAC
gnomAD
TCGA novel 12 G>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs772236698
CA10540178
14 I>M No ClinGen
ExAC
gnomAD
TCGA novel 15 G>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1438644948
CA415266346
16 C>W No ClinGen
gnomAD
CA10540179
rs747267730
17 K>Q No ClinGen
ExAC
gnomAD
TCGA novel 19 P>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA415266366
rs1190783820
20 Q>E No ClinGen
TOPMed
CA10540180
rs771355848
20 Q>L No ClinGen
ExAC
gnomAD
rs368281686
CA10540181
21 P>A No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs760172323
CA10540182
23 Y>H No ClinGen
ExAC
gnomAD
rs376483511
CA10540183
25 P>L No ClinGen
ExAC
TOPMed
gnomAD
rs376483511
CA415266401
25 P>Q No ClinGen
ExAC
TOPMed
gnomAD
rs376483511
CA415266402
25 P>R No ClinGen
ExAC
TOPMed
gnomAD
rs1338727042
CA415266404
26 A>P No ClinGen
gnomAD
rs1042295670
CA337194871
27 L>V No ClinGen
gnomAD
TCGA novel 31 M>missing Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
COSM272004
rs903144898
CA337194881
31 M>I large_intestine [Cosmic] No ClinGen
cosmic curated
Ensembl
CA10540185
rs370000417
31 M>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs763596159
CA10540186
32 F>L No ClinGen
ExAC
TOPMed
gnomAD
rs1352646124
CA415266450
33 C>G No ClinGen
gnomAD
rs751230928
CA10540187
33 C>S No ClinGen
ExAC
TOPMed
gnomAD
CA10540189
rs372712912
COSM1556770
34 A>E lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA337194890
rs1002895906
34 A>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
CA415266459
rs372712912
34 A>V Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs756110895
CA10540191
35 M>I No ClinGen
ExAC
gnomAD
CA415266470
rs1178926721
36 V>F No ClinGen
TOPMed
gnomAD
rs1178926721
CA415266468
36 V>I No ClinGen
TOPMed
gnomAD
CA337194949
rs189225995
38 T>I No ClinGen
1000Genomes
TOPMed
gnomAD
rs189225995
CA337194948
38 T>S No ClinGen
1000Genomes
TOPMed
gnomAD
rs374835856
CA10540192
39 I>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA337194972
rs780149081
41 V>I No ClinGen
Ensembl
rs1358231512
CA415266507
42 D>V No ClinGen
gnomAD
rs1178684632
CA415266523
45 G>R No ClinGen
gnomAD
CA415266532
rs1335216965
46 N>S No ClinGen
TOPMed
gnomAD
rs1446114524
CA415266545
48 M>T No ClinGen
gnomAD
rs748115693
CA10540193
48 M>V No ClinGen
ExAC
gnomAD
CA415266552
rs1431717214
49 V>F No ClinGen
TOPMed
rs777815917
CA10540195
50 I>V No ClinGen
ExAC
CA10540198
rs200181373
54 T>M No ClinGen
ExAC
TOPMed
gnomAD
CA10540197
rs200181373
54 T>R No ClinGen
ExAC
TOPMed
gnomAD
rs1408736639
CA415266588
55 K>T No ClinGen
gnomAD
TCGA novel 56 N>Y Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs776077410
CA337195007
57 K>N No ClinGen
ExAC
TOPMed
gnomAD
rs770481834
CA10540200
57 K>R No ClinGen
ExAC
TOPMed
gnomAD
CA415266609
rs1256061059
58 K>E No ClinGen
gnomAD
CA10540204
COSM267855
rs375887607
60 R>Q large_intestine [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
TOPMed
gnomAD
CA10540203
rs372854533
60 R>W No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs760418647
CA10540226
65 I>V No ClinGen
ExAC
TOPMed
gnomAD
rs766181640
COSM1132374
CA10540227
67 V>M prostate [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
CA10540229
rs759561321
73 A>D No ClinGen
ExAC
gnomAD
CA10540228
rs753699132
73 A>S No ClinGen
ExAC
gnomAD
CA10540230
rs764080839
74 D>N No ClinGen
ExAC
TOPMed
gnomAD
CA415266729
rs1569566965
75 M>K No ClinGen
Ensembl
rs751723921
CA10540231
77 V>G No ClinGen
ExAC
gnomAD
rs371241834
CA337196463
77 V>M No ClinGen
ESP
CA10540232
rs757426689
78 A>T No ClinGen
ExAC
gnomAD
CA415266778
rs1486773032
83 P>T No ClinGen
gnomAD
CA337196505
rs908301393
85 M>I No ClinGen
Ensembl
CA415266799
rs1389763290
86 L>M No ClinGen
TOPMed
rs1243406118
CA415266803
86 L>P No ClinGen
gnomAD
COSM3708482
rs1284467175
CA415266822
89 M>T liver [Cosmic] No ClinGen
cosmic curated
gnomAD
rs868643109
CA337196510
90 S>F Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs868643109
CA415266831
90 S>Y No ClinGen
gnomAD
CA10540233
rs781499377
91 I>T No ClinGen
ExAC
gnomAD
CA415266842
rs750707900
92 G>A No ClinGen
ExAC
TOPMed
gnomAD
rs750707900
CA415266841
92 G>E No ClinGen
ExAC
TOPMed
gnomAD
CA10540234
rs750707900
92 G>V No ClinGen
ExAC
TOPMed
gnomAD
CA415266846
rs769016022
93 G>A No ClinGen
1000Genomes
ExAC
gnomAD
CA10540235
rs769016022
93 G>D No ClinGen
1000Genomes
ExAC
gnomAD
CA10540236
rs780505218
96 L>P No ClinGen
ExAC
TOPMed
gnomAD
CA415266884
rs1440804421
98 Q>H No ClinGen
gnomAD
rs769263824
CA10540238
103 M>I No ClinGen
ExAC
gnomAD
rs376093395
CA10540237
103 M>V No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs771598289
CA10540241
105 G>E No ClinGen
ExAC
gnomAD
CA10540240
rs747586113
105 G>R No ClinGen
ExAC
TOPMed
gnomAD
rs772799343
CA10540242
108 T>K No ClinGen
ExAC
gnomAD
rs1394979471
CA415266956
109 G>E No ClinGen
gnomAD
TCGA novel 112 V>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs772438504
CA415266985
114 G>C No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA10540245
rs772438504
114 G>S No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA10540246
rs759381821
114 G>V No ClinGen
ExAC
gnomAD
CA10540247
rs765167544
116 I>L No ClinGen
ExAC
gnomAD
CA415266997
rs1240165897
116 I>T No ClinGen
TOPMed
gnomAD
rs1569566967
CA415267003
117 F>Y No ClinGen
Ensembl
CA415267012
rs1263043976
118 N>S No ClinGen
gnomAD
rs1199952495
CA415267025
120 V>M No ClinGen
gnomAD
CA415267046
rs767729782
123 A>G No ClinGen
ExAC
TOPMed
gnomAD
CA415267042
rs1462706023
123 A>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
CA10540250
rs767729782
123 A>V No ClinGen
ExAC
TOPMed
gnomAD
rs750653111
CA10540251
124 I>V No ClinGen
ExAC
gnomAD
rs766638424
CA10540253
125 N>S No ClinGen
ExAC
TOPMed
gnomAD
CA10540254
rs754172257
126 R>C No ClinGen
ExAC
TOPMed
gnomAD
CA415267062
rs755302073
COSM355790
126 R>H lung [Cosmic] No ClinGen
cosmic curated
ExAC
gnomAD
rs755302073
CA10540255
126 R>P No ClinGen
ExAC
gnomAD
TCGA novel 133 S>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10540256
rs779432297
134 L>R No ClinGen
ExAC
gnomAD
rs377409392
CA10540258
137 E>K Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs764196997
CA415267148
138 R>P No ClinGen
gnomAD
rs764196997
CA337196727
138 R>Q No ClinGen
gnomAD
rs900102278
CA337196719
138 R>W Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
CA415267152
rs1392354484
139 I>F No ClinGen
gnomAD
CA337196732
rs1042955180
140 F>S No ClinGen
Ensembl
CA415267169
rs1309528719
141 S>N No ClinGen
gnomAD
CA415267167
rs1309528719
141 S>T No ClinGen
gnomAD
CA415267180
rs1329859807
143 R>C No ClinGen
gnomAD
COSM3390481
rs370115563
CA10540259
143 R>H pancreas [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
TOPMed
gnomAD
rs746663885
CA10540260
144 N>D No ClinGen
ExAC
TOPMed
gnomAD
CA10540261
rs770679290
148 Y>H No ClinGen
ExAC
gnomAD
TCGA novel 149 L>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs745610748
CA10540263
150 V>F No ClinGen
ExAC
gnomAD
rs775520411
CA10540265
157 V>F No ClinGen
ExAC
TOPMed
gnomAD
CA10540266
rs775520411
157 V>I No ClinGen
ExAC
TOPMed
gnomAD
CA415267299
rs1432384935
162 P>T No ClinGen
gnomAD
CA10540269
rs760683612
164 M>T No ClinGen
ExAC
TOPMed
gnomAD
CA10540270
rs766555392
168 T>I No ClinGen
ExAC
gnomAD
TCGA novel 168 T>P Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10540271
rs754033816
169 I>F No ClinGen
ExAC
gnomAD
rs367944030
CA10540272
169 I>T No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs372045629
CA10540274
170 E>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs755414121
CA337196863
172 D>G No ClinGen
TOPMed
gnomAD
CA10540276
rs374353730
172 D>N Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1446061909
CA415267381
174 R>C No ClinGen
TOPMed
CA10540277
rs201701013
174 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA10540278
rs756727614
177 T>I No ClinGen
ExAC
TOPMed
gnomAD
rs753060369
CA337196909
178 C>R No ClinGen
gnomAD
CA10540279
rs766762255
184 N>Y No ClinGen
1000Genomes
ExAC
gnomAD
rs780037380
CA10540282
190 V>A No ClinGen
ExAC
TOPMed
gnomAD
rs1192300901
CA415267502
192 I>T No ClinGen
gnomAD
rs768655839
COSM206074
CA10540284
193 V>I Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
CA415267522
rs1162317136
195 I>T No ClinGen
TOPMed
gnomAD
CA10540285
rs202126801
196 H>N No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
TCGA novel 198 V>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10540287
COSM1466315
rs770934441
198 V>I Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
CA415267540
rs770934441
198 V>L No ClinGen
ExAC
gnomAD
CA415267548
rs1368018425
199 L>P Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs1318729967
CA415267571
203 I>V No ClinGen
gnomAD
CA415267577
rs1288793743
204 V>M Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs759714911
CA10540289
205 G>A No ClinGen
ExAC
gnomAD
TCGA novel 207 C>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1172874873
CA415267598
207 C>Y No ClinGen
TOPMed
rs1310902519
CA415267607
208 Y>C No ClinGen
gnomAD
CA337197014
rs367648979
209 V>M Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs765579691
CA10540290
217 A>E No ClinGen
ExAC
TOPMed
gnomAD
rs765579691
CA10540291
217 A>V Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
TCGA novel 218 A>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10540294
rs764521707
219 R>C No ClinGen
ExAC
TOPMed
gnomAD
CA415267675
rs1215052835
219 R>H No ClinGen
gnomAD
CA10540293
rs764521707
219 R>S No ClinGen
ExAC
TOPMed
gnomAD
CA415267696
rs1486584592
222 A>V No ClinGen
gnomAD
rs780617050
CA415267698
CA10540296
223 G>R No ClinGen
ExAC
gnomAD
rs965148805
CA337197110
226 P>L No ClinGen
Ensembl
rs750061222
CA10540297
227 D>H No ClinGen
ExAC
gnomAD
CA10540298
rs755778249
227 D>V No ClinGen
ExAC
rs1489440959
CA415267732
228 N>H No ClinGen
TOPMed
CA415267756
rs1418241293
231 A>G No ClinGen
gnomAD
rs749023791
CA10540300
233 V>F No ClinGen
ExAC
gnomAD
rs768602851
CA10540301
234 R>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA415267773
rs1433023729
234 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs1301101684
CA415267798
238 T>A No ClinGen
gnomAD
CA415267831
rs1602728326
242 I>N No ClinGen
Ensembl
rs1453734375
CA415267834
243 F>L No ClinGen
TOPMed
gnomAD
rs1489618662
CA415267842
244 L>V No ClinGen
gnomAD
CA10540303
rs748081183
247 A>T No ClinGen
ExAC
gnomAD
rs1268568172
CA415267868
248 V>L No ClinGen
TOPMed
TCGA novel 248 V>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA415267908
rs776638905
253 I>M No ClinGen
ExAC
TOPMed
gnomAD
rs921054298
CA337197162
253 I>V No ClinGen
Ensembl
CA415267910
rs1269174978
254 N>D No ClinGen
gnomAD
CA10540307
rs201906872
255 V>M No ClinGen
ExAC
gnomAD
CA415267924
rs1241914898
256 L>F Variant assessed as Somatic; 6.362e-05 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA415267943
rs1432829996
259 L>S No ClinGen
TOPMed
CA10540310
rs764464450
261 A>S No ClinGen
ExAC
gnomAD
CA337197258
rs944098807
264 P>L No ClinGen
TOPMed
rs1409366851
CA415267981
265 K>R No ClinGen
gnomAD
rs899987604
CA337197302
266 E>D No ClinGen
TOPMed
gnomAD
CA415267996
rs1174566357
267 M>T No ClinGen
gnomAD
rs1187647008
CA415268001
268 A>T No ClinGen
TOPMed
CA415268007
rs1160433224
269 G>S No ClinGen
gnomAD
CA415268017
rs1405510846
270 K>R No ClinGen
gnomAD
rs934598464
CA337197322
272 P>S No ClinGen
Ensembl
CA415268038
CA10540315
rs755686782
273 N>K No ClinGen
ExAC
gnomAD
CA10540314
rs369378152
273 N>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA415268058
rs1422848790
276 Y>C No ClinGen
TOPMed
gnomAD
CA415268067
rs1374888611
277 L>P No ClinGen
gnomAD
rs746633698
CA337197338
279 A>V No ClinGen
Ensembl
rs1441248107
CA415268080
280 Y>H No ClinGen
gnomAD
TCGA novel 281 F>missing Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1210914246
CA415268102
283 A>T No ClinGen
TOPMed
rs1304969433
CA415268105
283 A>V No ClinGen
gnomAD
CA337197340
rs770761959
288 C>S No ClinGen
TOPMed
gnomAD
rs753563400
CA10540317
290 N>D No ClinGen
ExAC
gnomAD
rs754798475
COSM161361
CA10540318
290 N>S breast [Cosmic] No ClinGen
cosmic curated
ExAC
gnomAD
rs748110682
CA10540320
291 A>G No ClinGen
ExAC
gnomAD
CA415268192
rs894022568
296 L>F No ClinGen
TOPMed
rs745869992
CA10540323
296 L>P No ClinGen
ExAC
gnomAD
CA337197361
rs894022568
296 L>V No ClinGen
TOPMed
COSM3843874
CA10540325
rs745374692
302 R>Q Variant assessed as Somatic; 0.0 impact. breast [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
TCGA novel 303 R>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1303292431
CA415268252
305 Y>N No ClinGen
TOPMed
CA10540326
rs749565001
306 W>R No ClinGen
ExAC
gnomAD
CA10540327
rs768981366
310 H>Y No ClinGen
ExAC
TOPMed
gnomAD
CA10540330
rs767842076
313 R>Q No ClinGen
ExAC
gnomAD
rs376836037
CA10540328
313 R>W No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA415268332
rs1215388278
316 I>T No ClinGen
Ensembl
rs1224309221
CA415268347
318 F>C No ClinGen
gnomAD
CA337197446
rs1046919874
322 L>V No ClinGen
Ensembl
TCGA novel 325 D>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10540333
rs766036345
326 I>T No ClinGen
ExAC
gnomAD
rs751147111
CA10540334
COSM1253564
327 R>C Variant assessed as Somatic; 0.0 impact. oesophagus [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
1000Genomes
ExAC
NCI-TCGA
gnomAD
rs1433987045
CA415268406
327 R>P No ClinGen
gnomAD
CA10540336
rs754743441
330 Q>* No ClinGen
ExAC
gnomAD
CA10540338
rs374473359
330 Q>H No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10540337
rs199826607
330 Q>P No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA415268440
rs1275698711
332 A>P No ClinGen
gnomAD
COSM456968
CA337197479
rs200075966
333 R>C Variant assessed as Somatic; 0.0 impact. breast [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
COSM1466321
rs370344133
CA10540341
333 R>H Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs370344133
CA10540340
333 R>P No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs756168251
CA10540342
334 T>S No ClinGen
ExAC
gnomAD
rs749509959
CA10540344
335 L>Q No ClinGen
ExAC
gnomAD
CA10540343
rs780151060
335 L>V No ClinGen
ExAC
gnomAD
CA10540345
rs200876781
336 A>D Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
gnomAD
CA10540346
rs774635473
337 R>C No ClinGen
ExAC
TOPMed
gnomAD
rs774635473
CA10540347
337 R>G No ClinGen
ExAC
TOPMed
gnomAD
CA10540348
rs375512067
337 R>H No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs370636515
COSM3800466
CA10540350
338 A>T urinary_tract [Cosmic] No ClinGen
cosmic curated
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10540351
rs765982317
339 R>C No ClinGen
ExAC
TOPMed
gnomAD
COSM1166381
CA10540353
rs779386501
339 R>H Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
rs779386501
CA415268471
339 R>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs779386501
CA10540352
339 R>P No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA415268469
rs765982317
339 R>S Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
TCGA novel
CA415268483
rs1602728624
341 H>L Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
Ensembl
CA10540354
rs764731190
343 R>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs752426790
CA10540356
343 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
CA10540355
rs752426790
343 R>P No ClinGen
ExAC
gnomAD
rs757255062
CA10540359
344 D>N No ClinGen
ExAC
TOPMed
gnomAD
rs780097558
CA10540360
COSM1116875
347 R>C endometrium [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
CA10540361
rs780097558
347 R>G No ClinGen
ExAC
TOPMed
gnomAD
rs748432654
CA10540362
COSM1660029
347 R>H kidney [Cosmic] No ClinGen
cosmic curated
1000Genomes
ExAC
gnomAD
CA10540363
rs778949621
348 E>K No ClinGen
ExAC
gnomAD
TCGA novel 350 D>Y Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
COSM1116878
rs374706343
CA10540364
351 R>C ovary endometrium [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
TOPMed
gnomAD
CA415268543
rs374706343
351 R>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs368374300
CA10540365
351 R>H No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
TCGA novel 352 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs762988621
CA10540366
353 H>Y No ClinGen
ExAC
gnomAD
rs771505568
CA10540369
355 C>S No ClinGen
ExAC
TOPMed
gnomAD
rs771505568
CA415268569
355 C>Y No ClinGen
ExAC
TOPMed
gnomAD
rs866633030
CA337197666
356 P>L No ClinGen
Ensembl
rs1193925783
CA415268574
356 P>S No ClinGen
gnomAD
CA337197687
rs944166563
357 A>G No ClinGen
TOPMed
CA10540370
rs778133759
361 T>I No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs370666513
CA10540371
362 P>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs370666513
CA415268613
362 P>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA337197724
rs868778152
364 N>K No ClinGen
Ensembl
rs1351459215
CA415268627
364 N>S No ClinGen
TOPMed
rs1356454277
CA415268632
365 V>A No ClinGen
gnomAD
rs374566932
CA10540372
365 V>I Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA10540374
rs200814649
366 R>G No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA10540375
rs372169533
366 R>Q Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs200814649
CA10540373
366 R>W Variant assessed as Somatic; 6.321e-05 impact. [NCI-TCGA] No ClinGen
1000Genomes
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1388194559
CA415268641
367 N>S No ClinGen
TOPMed
TCGA novel 368 V>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1319644027
CA415268660
370 L>S No ClinGen
TOPMed
gnomAD
CA10540377
rs761612420
371 P>A No ClinGen
ExAC
gnomAD
rs1419443084
CA415268674
372 G>D No ClinGen
TOPMed
TCGA novel 372 G>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10540378
rs771135593
373 D>G No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA10540379
rs750380397
374 A>T No ClinGen
ExAC
gnomAD
CA415268697
rs1259504880
376 A>G No ClinGen
gnomAD
rs866664291
CA337197788
377 G>D No ClinGen
Ensembl
CA10540380
rs754987273
378 H>Q No ClinGen
ExAC
gnomAD
CA10540381
rs779086754
379 P>S No ClinGen
ExAC
TOPMed
gnomAD
rs1243956072
CA415268719
380 D>G Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
CA10540382
rs375105847
380 D>N Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs867872295
CA337197817
381 R>C No ClinGen
TOPMed
gnomAD
rs758704622
CA10540383
381 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
CA10540384
rs778153451
382 A>T No ClinGen
ExAC
gnomAD
rs747308998
CA10540385
383 S>F No ClinGen
ExAC
gnomAD
CA10540386
rs367675848
384 G>A No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10540387
rs367675848
384 G>D No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA337197879
rs934589886
386 P>A No ClinGen
TOPMed
CA10540388
rs746436765
386 P>R No ClinGen
ExAC
gnomAD
TCGA novel 389 H>Y Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs989144884
CA337197880
390 S>C No ClinGen
Ensembl
rs776809214
CA10540389
392 S>F Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
gnomAD
CA10540390
rs200132458
394 S>F No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10540392
rs768242890
397 R>C No ClinGen
ExAC
gnomAD
COSM1556760
rs200441669
CA10540393
397 R>H lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
1000Genomes
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs200441669
CA10540394
397 R>L No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs906180998
CA337197906
398 K>R No ClinGen
TOPMed
CA10540396
rs750325375
399 S>A No ClinGen
ExAC
gnomAD
CA337197925
rs1003331674
400 A>T No ClinGen
TOPMed
gnomAD
CA10540397
rs760732722
400 A>V Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
CA10540399
rs775392711
402 T>I No ClinGen
1000Genomes
ExAC
gnomAD
rs913866571
CA337197940
403 H>Y No ClinGen
TOPMed
gnomAD
rs762651170
CA10540400
405 K>E No ClinGen
1000Genomes
ExAC
gnomAD
rs1175281026
CA415268871
406 S>A No ClinGen
gnomAD
CA415268880
rs1249628497
407 V>D No ClinGen
TOPMed
gnomAD
CA337197950
rs868561933
408 F>S No ClinGen
Ensembl
rs764372963
CA10540401
409 S>R No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 411 S>C Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
COSM1556756
rs1479836440
CA415268919
413 A>D lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
rs781719205
CA10540404
413 A>T No ClinGen
ExAC
gnomAD
TCGA novel 414 A>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs201019474
CA337197980
415 S>C No ClinGen
Ensembl
CA10540405
rs746360125
416 G>S No ClinGen
ExAC
gnomAD
CA415268943
rs1460097329
417 H>P No ClinGen
gnomAD
CA415268944
rs369656707
417 H>Q No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs780441239
CA10540408
419 K>N No ClinGen
ExAC
gnomAD
CA10540409
rs748768797
420 P>L No ClinGen
ExAC
TOPMed
gnomAD
CA10540410
rs768173691
421 V>A No ClinGen
ExAC
gnomAD
CA415268985
rs1283942989
424 H>R No ClinGen
gnomAD
CA415268981
rs1222989275
424 H>Y No ClinGen
gnomAD
CA10540412
rs773967847
426 K>N No ClinGen
ExAC
rs764148668
CA337198012
427 P>S No ClinGen
1000Genomes
TOPMed
rs751456462
CA337198013
428 A>V No ClinGen
1000Genomes
CA415269021
rs1199665709
430 G>V No ClinGen
gnomAD
rs200542186
CA337198015
432 P>S No ClinGen
1000Genomes
TOPMed
rs1476960884
CA415269044
433 K>N No ClinGen
TOPMed
TCGA novel 434 S>Y Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 435 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1194090193
CA415269073
438 Y>C No ClinGen
TOPMed
CA10540414
rs771845794
439 P>L No ClinGen
ExAC
gnomAD
TCGA novel 440 K>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1485316930
CA415269091
441 P>A No ClinGen
TOPMed
CA337198018
rs768332458
443 S>P No ClinGen
gnomAD
rs766271002
CA10540418
446 F>L No ClinGen
ExAC
gnomAD
rs1033847876
CA337198029
447 K>R No ClinGen
TOPMed
CA337198036
rs377039209
448 A>D No ClinGen
ESP
TOPMed
rs377039209
CA415269136
448 A>G No ClinGen
ESP
TOPMed
CA337198035
rs374023233
448 A>P No ClinGen
ESP
TOPMed
rs374023233
CA337198034
448 A>T No ClinGen
ESP
TOPMed
rs763041518
CA10540421
449 D>A No ClinGen
ExAC
TOPMed
gnomAD
rs1340399540
CA415269155
451 V>A No ClinGen
TOPMed
rs1332704667
CA415269166
453 F>L No ClinGen
TOPMed
TCGA novel 453 F>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA415269185
rs1373241610
455 G>A No ClinGen
gnomAD
rs370024017
CA10540422
457 S>P No ClinGen
ESP
ExAC
gnomAD
CA337198058
rs374455722
459 H>R No ClinGen
ESP
TOPMed
CA415269234
rs1310170870
462 P>L No ClinGen
gnomAD
rs1403084993
CA415269236
463 D>H No ClinGen
TOPMed
rs757621208
CA10540424
473 N>D No ClinGen
ExAC
TOPMed
gnomAD
CA10540425
rs767985802
474 P>A No ClinGen
ExAC
TOPMed
gnomAD
rs938114534
CA337198128
479 G>S No ClinGen
Ensembl
CA415269352
rs1308258094
480 H>R No ClinGen
gnomAD
CA10540427
rs370262045
481 H>N No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs749806993
CA10540429
481 H>R No ClinGen
ExAC
gnomAD
CA10540428
rs370262045
481 H>Y No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 483 S>P Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA337198186
rs1027467005
484 A>D Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
CA10540431
rs778458448
484 A>P No ClinGen
ExAC
TOPMed
gnomAD
CA10540432
rs747785501
486 S>R No ClinGen
ExAC
gnomAD
CA415269406
rs1458835474
489 K>E No ClinGen
TOPMed
rs771655329
CA10540433
490 S>P No ClinGen
ExAC
gnomAD
CA415269428
rs1258222932
492 F>S No ClinGen
TOPMed
rs772742529
CA10540434
493 S>G No ClinGen
ExAC
gnomAD
CA10540435
rs62620754
493 S>N No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
TCGA novel 495 A>P Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs770656377
CA10540436
496 T>A No ClinGen
ExAC
TOPMed
gnomAD
CA10540437
rs776610833
496 T>S No ClinGen
ExAC
TOPMed
gnomAD
CA415269457
rs1341574142
497 S>N No ClinGen
TOPMed
rs1410742879
CA415269474
499 P>L No ClinGen
gnomAD
CA415269485
rs764266376
501 P>S No ClinGen
ExAC
TOPMed
gnomAD
CA10540439
rs764266376
501 P>T No ClinGen
ExAC
TOPMed
gnomAD
rs199797606
CA337198243
502 T>I No ClinGen
1000Genomes
VAR_062254 502 T>del lower fasting circulating triglyceride levels [UniProt] No UniProt
CA337198248
rs868254928
504 G>A No ClinGen
Ensembl
CA337198255
rs868254928
504 G>D No ClinGen
Ensembl
rs200787393
CA337198261
505 H>P No ClinGen
Ensembl
CA10540441
rs772097142
507 K>GGGIEGSKTE* No ClinGen
ExAC
rs1569566969
CA415269547
509 A>V No ClinGen
Ensembl
rs995790572
CA337198268
510 T>P No ClinGen
Ensembl
rs998246004
CA337198269
511 S>G No ClinGen
TOPMed
CA415269569
rs1428757714
512 H>P No ClinGen
TOPMed
gnomAD
CA415269570
rs1428757714
512 H>R No ClinGen
TOPMed
gnomAD
TCGA novel 514 E>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs867249936
CA337198289
514 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
Ensembl
NCI-TCGA
rs1388397532
CA415269591
515 P>L Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
rs1325738390
CA415269612
519 D>N No ClinGen
gnomAD
CA10540446
rs750644483
520 Y>C No ClinGen
ExAC
gnomAD
rs767714298
CA10540445
520 Y>N No ClinGen
ExAC
TOPMed
gnomAD
rs766691601
CA10540448
521 P>R No ClinGen
ExAC
TOPMed
gnomAD
CA10540451
rs779405352
522 K>N No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 523 P>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1238236399
CA415269646
524 A>S No ClinGen
TOPMed
rs752135038
CA10540452
526 T>S No ClinGen
ExAC
gnomAD
CA415269665
rs1242117442
527 S>N No ClinGen
gnomAD
CA10540455
rs777433829
527 S>R No ClinGen
ExAC
gnomAD
TCGA novel 528 H>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA415269681
rs1602729266
529 P>L No ClinGen
Ensembl
VAR_062255
rs561077
CA10540457
532 T>A higher fasting circulating triglyceride levels [UniProt] No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
rs374366140
CA337198335
536 N>S No ClinGen
ESP
TOPMed
TCGA novel 542 S>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 544 C>Y Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs917168816
CA337198344
545 P>S No ClinGen
TOPMed
gnomAD
rs371146604
CA10540461
546 E>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1379288417
CA415269796
547 I>F No ClinGen
TOPMed
rs1310076466
CA415269808
549 A>P No ClinGen
TOPMed
CA10540462
rs758699310
550 I>V No ClinGen
1000Genomes
ExAC
gnomAD
TCGA novel 551 A>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10540464
rs760868835
552 H>P No ClinGen
ExAC
gnomAD
CA10540466
rs182874490
552 H>Q No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs760868835
CA10540465
552 H>R No ClinGen
ExAC
gnomAD
rs773450160
CA10540463
552 H>Y No ClinGen
ExAC
TOPMed
gnomAD
CA10540468
COSM1116900
rs765690309
557 D>N Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
TCGA novel 560 L>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA415269901
rs757882661
563 S>* No ClinGen
ExAC
TOPMed
gnomAD
CA10540470
rs757882661
563 S>L No ClinGen
ExAC
TOPMed
gnomAD
CA10540472
rs751220560
564 A>T No ClinGen
ExAC
gnomAD
CA415269911
rs1211277206
565 S>Y No ClinGen
gnomAD
CA10540473
rs202029963
567 P>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA415269936
rs1409297036
569 A>G No ClinGen
gnomAD
CA10540475
rs745595243
569 A>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA10540476
rs769745013
571 P>S No ClinGen
ExAC
gnomAD
rs1602729404
CA415269963
574 P>T No ClinGen
Ensembl
rs1478299922
CA415269980
576 A>V No ClinGen
gnomAD
CA10540477
rs780093398
577 S>N No ClinGen
ExAC
gnomAD
CA415269994
rs749275695
578 Q>H No ClinGen
ExAC
gnomAD
TCGA novel 580 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA10540479
rs371707915
583 T>A No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs901402971
CA337198468
583 T>S No ClinGen
Ensembl
CA10540481
rs760818840
585 A>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA415270040
rs1280087906
586 D>H No ClinGen
gnomAD
TCGA novel 586 D>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA415270048
rs1352212265
587 L>V No ClinGen
gnomAD
rs765410234
CA337198494
588 P>S No ClinGen
Ensembl
CA415270070
rs1282024314
590 P>L No ClinGen
gnomAD
CA10540483
rs770991631
590 P>S No ClinGen
ExAC
gnomAD
rs1220659137
CA415270077
592 V>I No ClinGen
gnomAD
CA415270096
rs1436476672
595 T>A No ClinGen
gnomAD
rs1204220421
CA415270123
599 D>N No ClinGen
TOPMed
gnomAD
CA415270138
rs1253174231
600 Y>* No ClinGen
gnomAD
CA337198522
rs866973433
601 H>Q No ClinGen
Ensembl
CA337198562
rs201645456
604 V>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA10540486
rs201645456
604 V>M No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA415270164
rs1197882347
605 V>I No ClinGen
gnomAD
CA10540487
VAR_062256
rs13440581
606 I>V higher fasting circulating triglyceride levels [UniProt] No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
rs1478378985
CA415270190
609 E>K No ClinGen
gnomAD
CA10540488
rs763439576
610 D>G No ClinGen
ExAC
TOPMed
gnomAD
COSM755928
rs763647516
CA10540489
612 P>S lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
CA10540490
rs750977314
617 V>M Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs756799778
CA10540491
618 V>W No ClinGen
ExAC
gnomAD

No associated diseases with Q13585

1 regional properties for Q13585

Type Name Position InterPro Accession
domain GPCR, rhodopsin-like, 7TM 71 - 396 IPR017452

Functions

Description
EC Number
Subcellular Localization
  • Cell membrane ; Multi-pass membrane protein
  • Postsynaptic density
  • ;
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

3 GO annotations of cellular component

Name Definition
integral component of plasma membrane The component of the plasma membrane consisting of the gene products and protein complexes having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane.
nucleoplasm That part of the nuclear content other than the chromosomes or the nucleolus.
plasma membrane The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins.

2 GO annotations of molecular function

Name Definition
G protein-coupled receptor activity Combining with an extracellular signal and transmitting the signal across the membrane by activating an associated G-protein; promotes the exchange of GDP for GTP on the alpha subunit of a heterotrimeric G-protein complex.
melatonin receptor activity Combining with melatonin, N-acetyl-5-methoxytryptamine, to initiate a change in cell activity. Melatonin is a neuroendocrine substance that stimulates the aggregation of melanosomes in melanophores, thus lightening the skin.

2 GO annotations of biological process

Name Definition
cell-cell signaling Any process that mediates the transfer of information from one cell to another. This process includes signal transduction in the receiving cell and, where applicable, release of a ligand and any processes that actively facilitate its transport and presentation to the receiving cell. Examples include signaling via soluble ligands, via cell adhesion molecules and via gap junctions.
G protein-coupled receptor signaling pathway The series of molecular signals initiated by a ligand binding to its receptor, in which the activated receptor promotes the exchange of GDP for GTP on the alpha-subunit of an associated heterotrimeric G-protein complex. The GTP-bound activated alpha-G-protein then dissociates from the beta- and gamma-subunits to further transmit the signal within the cell. The pathway begins with receptor-ligand interaction, and ends with regulation of a downstream cellular process. The pathway can start from the plasma membrane, Golgi or nuclear membrane.

120 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
Q2YDN1 GPR161 G protein-coupled receptor 161 Bos taurus (Bovine) PR
Q0GBZ5 HCRTR1 Orexin/Hypocretin receptor type 1 Bos taurus (Bovine) PR
Q17QD8 GPR37L1 G-protein coupled receptor 37-like 1 Bos taurus (Bovine) PR
Q8SPN1 PROKR2 Prokineticin receptor 2 Bos taurus (Bovine) PR
P46626 ADRB3 Beta-3 adrenergic receptor Bos taurus (Bovine) PR
O46639 TRHR Thyrotropin-releasing hormone receptor Bos taurus (Bovine) PR
Q8SPN2 PROKR1 Prokineticin receptor 1 Bos taurus (Bovine) PR
B9VR26 CMLKR1 Chemerin-like receptor 1 Bos taurus (Bovine) PR
P18130 ADRA1A Alpha-1A adrenergic receptor Bos taurus (Bovine) PR
B4XF06 GPR39 G-protein coupled receptor 39 Bos taurus (Bovine) PR
O18913 OPN1LW Long-wave-sensitive opsin 1 Felis catus (Cat) (Felis silvestris catus) PR
P28683 PRA1 Green-sensitive opsin Gallus gallus (Chicken) PR
Q9N298 HTR1A 5-hydroxytryptamine receptor 1A Pan troglodytes (Chimpanzee) PR
P08099 Rh2 Opsin Rh2 Drosophila melanogaster (Fruit fly) PR
P06002 ninaE Opsin Rh1 Drosophila melanogaster (Fruit fly) PR
Q4LBB9 Octbeta2R Octopamine receptor beta-2R Drosophila melanogaster (Fruit fly) PR
Q8NFJ6 PROKR2 Prokineticin receptor 2 Homo sapiens (Human) PR
Q9BZJ6 GPR63 Probable G-protein coupled receptor 63 Homo sapiens (Human) PR
Q9H3N8 HRH4 Histamine H4 receptor Homo sapiens (Human) PR
P28336 NMBR Neuromedin-B receptor Homo sapiens (Human) PR
Q9Y5Y3 GPR45 Probable G-protein coupled receptor 45 Homo sapiens (Human) PR
P08913 ADRA2A Alpha-2A adrenergic receptor Homo sapiens (Human) PR
P41597 CCR2 C-C chemokine receptor type 2 Homo sapiens (Human) PR
P51681 CCR5 C-C chemokine receptor type 5 Homo sapiens (Human) PR
Q8TCW9 PROKR1 Prokineticin receptor 1 Homo sapiens (Human) PR
Q99788 CMKLR1 Chemerin-like receptor 1 Homo sapiens (Human) PR
P08908 HTR1A 5-hydroxytryptamine receptor 1A Homo sapiens (Human) PR
P30559 OXTR Oxytocin receptor Homo sapiens (Human) PR
P32239 CCKBR Gastrin/cholecystokinin type B receptor Homo sapiens (Human) PR
O60883 GPR37L1 G-protein coupled receptor 37-like 1 Homo sapiens (Human) PR
Q8TDU9 RXFP4 Relaxin-3 receptor 2 Homo sapiens (Human) PR
P04000 OPN1LW Long-wave-sensitive opsin 1 Homo sapiens (Human) PR
Q6U736 OPN5 Opsin-5 Homo sapiens (Human) PR
P34972 CNR2 Cannabinoid receptor 2 Homo sapiens (Human) PR
P24530 EDNRB Endothelin receptor type B Homo sapiens (Human) PR
P35348 ADRA1A Alpha-1A adrenergic receptor Homo sapiens (Human) PR
Q6W5P4 NPSR1 Neuropeptide S receptor Homo sapiens (Human) PR
O43613 HCRTR1 Orexin/Hypocretin receptor type 1 Homo sapiens (Human) PR
P61073 CXCR4 C-X-C chemokine receptor type 4 Homo sapiens (Human) PR
Q9BXC0 HCAR1 Hydroxycarboxylic acid receptor 1 Homo sapiens (Human) PR
Q15761 NPY5R Neuropeptide Y receptor type 5 Homo sapiens (Human) PR
Q8N6U8 GPR161 G-protein coupled receptor 161 Homo sapiens (Human) PR
Q6DWJ6 GPR139 Probable G-protein coupled receptor 139 Homo sapiens (Human) PR
P21462 FPR1 fMet-Leu-Phe receptor Homo sapiens (Human) PR
P46091 CMKLR2 Chemerin-like receptor 2 Homo sapiens (Human) PR
P32745 SSTR3 Somatostatin receptor type 3 Homo sapiens (Human) PR
P41439 FOLR3 Folate receptor gamma Homo sapiens (Human) PR
P30556 AGTR1 Type-1 angiotensin II receptor Homo sapiens (Human) PR
P35414 APLNR Apelin receptor Homo sapiens (Human) PR
P30411 BDKRB2 B2 bradykinin receptor Homo sapiens (Human) PR
P19973 Lsp1 Lymphocyte-specific protein 1 Mus musculus (Mouse) PR
O54799 Nmbr Neuromedin-B receptor Mus musculus (Mouse) PR
Q64264 Htr1a 5-hydroxytryptamine receptor 1A Mus musculus (Mouse) PR
P51675 Ccr1 C-C chemokine receptor type 1 Mus musculus (Mouse) PR
Q5U431 Gpr39 G-protein coupled receptor 39 Mus musculus (Mouse) PR
Q99JG2 Gpr37l1 G-protein coupled receptor 37-like 1 Mus musculus (Mouse) PR
P97295 Npy2r Neuropeptide Y receptor type 2 Mus musculus (Mouse) PR
O08786 Cckar Cholecystokinin receptor type A Mus musculus (Mouse) PR
P56481 Cckbr Gastrin/cholecystokinin type B receptor Mus musculus (Mouse) PR
P30731 Gpr83 G-protein coupled receptor 83 Mus musculus (Mouse) PR
P97468 Cmklr1 Chemerin-like receptor 1 Mus musculus (Mouse) PR
P21761 Trhr Thyrotropin-releasing hormone receptor Mus musculus (Mouse) PR
Q5QD16 Taar3 Trace amine-associated receptor 3 Mus musculus (Mouse) PR
P97292 Hrh2 Histamine H2 receptor Mus musculus (Mouse) PR
Q9EQQ3 Gpr63 Probable G-protein coupled receptor 63 Mus musculus (Mouse) PR
Q924H0 Npffr2 Neuropeptide FF receptor 2 Mus musculus (Mouse) PR
P34971 Adrb1 Beta-1 adrenergic receptor Mus musculus (Mouse) PR
Q91ZY2 Hrh4 Histamine H4 receptor Mus musculus (Mouse) PR
O88416 Gpr33 Probable G-protein coupled receptor 33 Mus musculus (Mouse) PR
Q8K087 Cmklr2 Chemerin-like receptor 2 Mus musculus (Mouse) PR
P70658 Cxcr4 C-X-C chemokine receptor type 4 Mus musculus (Mouse) PR
Q9WV08 Aplnr Apelin receptor Mus musculus (Mouse) PR
P97718 Adra1a Alpha-1A adrenergic receptor Mus musculus (Mouse) PR
Q8BZP8 Npsr1 Neuropeptide S receptor Mus musculus (Mouse) PR
Q8K458 Prokr2 Prokineticin receptor 2 Mus musculus (Mouse) PR
P58308 Hcrtr2 Orexin receptor type 2 Mus musculus (Mouse) PR
Q7TQP3 Gpr119 Glucose-dependent insulinotropic receptor Mus musculus (Mouse) PR
Q8BGE9 Rxfp3 Relaxin-3 receptor 1 Mus musculus (Mouse) PR
Q6VZZ7 Opn5 Opsin-5 Mus musculus (Mouse) PR
Q8CIM5 Gpr84 G-protein coupled receptor 84 Mus musculus (Mouse) PR
P25962 Adrb3 Beta-3 adrenergic receptor Mus musculus (Mouse) PR
Q80UC8 Gpr139 Probable G-protein coupled receptor 139 Mus musculus (Mouse) PR
P0C5I1 Gpr25 Probable G-protein coupled receptor 25 Mus musculus (Mouse) PR
P47936 Cnr2 Cannabinoid receptor 2 Mus musculus (Mouse) PR
Q5QD13 Taar6 Trace amine-associated receptor 6 Mus musculus (Mouse) PR
P35846 Folr1 Folate receptor alpha Mus musculus (Mouse) PR
P58307 Hcrtr1 Orexin/Hypocretin receptor type 1 Mus musculus (Mouse) PR
Q8C131 Hcar1 Hydroxycarboxylic acid receptor 1 Mus musculus (Mouse) PR
Q9EQQ4 Gpr45 Probable G-protein coupled receptor 45 Mus musculus (Mouse) PR
B2RPY5 Gpr161 G-protein coupled receptor 161 Mus musculus (Mouse) PR
Q764M9 CXCR4 C-X-C chemokine receptor type 4 Sus scrofa (Pig) PR
Q9EQD2 Npffr2 Neuropeptide FF receptor 2 Rattus norvegicus (Rat) PR
O08565 Cxcr4 C-X-C chemokine receptor type 4 Rattus norvegicus (Rat) PR
Q01717 Trhr Thyrotropin-releasing hormone receptor Rattus norvegicus (Rat) PR
P30936 Sstr3 Somatostatin receptor type 3 Rattus norvegicus (Rat) PR
Q9JHG3 Aplnr Apelin receptor Rattus norvegicus (Rat) PR
P43140 Adra1a Alpha-1A adrenergic receptor Rattus norvegicus (Rat) PR
P19327 Htr1a 5-hydroxytryptamine receptor 1A Rattus norvegicus (Rat) PR
P56719 Hcrtr2 Orexin receptor type 2 Rattus norvegicus (Rat) PR
P28564 Htr1b 5-hydroxytryptamine receptor 1B Rattus norvegicus (Rat) PR
P56718 Hcrtr1 Orexin/Hypocretin receptor type 1 Rattus norvegicus (Rat) PR
P28647 Adora3 Adenosine receptor A3 Rattus norvegicus (Rat) PR
P25102 Hrh2 Histamine H2 receptor Rattus norvegicus (Rat) PR
P23944 Adra1d Alpha-1D adrenergic receptor Rattus norvegicus (Rat) PR
Q8R415 Prokr2 Prokineticin receptor 2 Rattus norvegicus (Rat) PR
Q5QD24 Taar3 Trace amine-associated receptor 3 Rattus norvegicus (Rat) PR
P0C0W8 Gpr139 Probable G-protein coupled receptor 139 Rattus norvegicus (Rat) PR
P35370 Oprl1 Nociceptin receptor Rattus norvegicus (Rat) PR
P46090 Cmklr2 Chemerin-like receptor 2 Rattus norvegicus (Rat) PR
O97664 CMKLR2 Chemerin-like receptor 2 Macaca mulatta (Rhesus macaque) PR
O97666 APLNR Apelin receptor Macaca mulatta (Rhesus macaque) PR
Q56H79 NPSR1 Neuropeptide S receptor Macaca mulatta (Rhesus macaque) PR
Q18904 npr-8 Probable G-protein coupled receptor npr-8 Caenorhabditis elegans PR
Q09388 gar-2 Muscarinic acetylcholine receptor gar-2 Caenorhabditis elegans PR
B3DM66 gpr161 G-protein coupled receptor 161 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
Q9W6A6 opn1mw4 Green-sensitive opsin-4 Danio rerio (Zebrafish) (Brachydanio rerio) PR
Q9W6A5 opn1mw1 Green-sensitive opsin-1 Danio rerio (Zebrafish) (Brachydanio rerio) PR
Q8AYM7 opn1mw3 Green-sensitive opsin-3 Danio rerio (Zebrafish) (Brachydanio rerio) PR
Q8AYN0 opn1lw2 Red-sensitive opsin-2 Danio rerio (Zebrafish) (Brachydanio rerio) PR
Q90X46 gpr161 G-protein coupled receptor 161 Danio rerio (Zebrafish) (Brachydanio rerio) PR
10 20 30 40 50 60
MGPTLAVPTP YGCIGCKLPQ PEYPPALIIF MFCAMVITIV VDLIGNSMVI LAVTKNKKLR
70 80 90 100 110 120
NSGNIFVVSL SVADMLVAIY PYPLMLHAMS IGGWDLSQLQ CQMVGFITGL SVVGSIFNIV
130 140 150 160 170 180
AIAINRYCYI CHSLQYERIF SVRNTCIYLV ITWIMTVLAV LPNMYIGTIE YDPRTYTCIF
190 200 210 220 230 240
NYLNNPVFTV TIVCIHFVLP LLIVGFCYVR IWTKVLAARD PAGQNPDNQL AEVRNFLTMF
250 260 270 280 290 300
VIFLLFAVCW CPINVLTVLV AVSPKEMAGK IPNWLYLAAY FIAYFNSCLN AVIYGLLNEN
310 320 330 340 350 360
FRREYWTIFH AMRHPIIFFS GLISDIREMQ EARTLARARA HARDQAREQD RAHACPAVEE
370 380 390 400 410 420
TPMNVRNVPL PGDAAAGHPD RASGHPKPHS RSSSAYRKSA STHHKSVFSH SKAASGHLKP
430 440 450 460 470 480
VSGHSKPASG HPKSATVYPK PASVHFKADS VHFKGDSVHF KPDSVHFKPA SSNPKPITGH
490 500 510 520 530 540
HVSAGSHSKS AFSAATSHPK PTTGHIKPAT SHAEPTTADY PKPATTSHPK PTAADNPELS
550 560 570 580 590 600
ASHCPEIPAI AHPVSDDSDL PESASSPAAG PTKPAASQLE SDTIADLPDP TVVTTSTNDY
610
HDVVVIDVED DPDEMAV