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

11 structures for Q16695

Entry ID Method Resolution Chain Position Source
2V1D X-ray 310 A C 2-22 PDB
2YBP X-ray 202 A C/D 31-42 PDB
2YBS X-ray 232 A C/D 31-42 PDB
3A6N X-ray 270 A A/E 1-136 PDB
3T6R X-ray 195 A D 2-8 PDB
4V2V X-ray 200 A C/D 26-30 PDB
4V2W X-ray 181 A C 17-36 PDB
6OIE X-ray 208 A C/D 2-20 PDB
6WAT X-ray 180 A A/B/C/D/E/F/G/H/I/J/K/L/M/N/O/P/Q/R/S/T/V/Y/Z/a/b/c/d/e/f/g 22-30 PDB
6WAU X-ray 175 A G/H/I/J/K/L 22-33 PDB
AF-Q16695-F1 Predicted AlphaFoldDB

233 variants for Q16695

Variant ID(s) Position Change Description Diseaes Association Provenance
CA345144764
rs774804205
2 A>G No ClinGen
ExAC
TOPMed
gnomAD
CA1441481
rs759975640
2 A>P No ExAC
TOPMed
gnomAD
ClinGen
CA1441480
rs759975640
2 A>S No ExAC
TOPMed
gnomAD
ClinGen
CA1441479
rs774804205
2 A>V No ClinGen
ExAC
TOPMed
gnomAD
CA1441477
rs150247684
3 R>* Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No 1000Genomes
ESP
ExAC
TOPMed
ClinGen
NCI-TCGA
CA345144757
rs150247684
3 R>G No 1000Genomes
ESP
ExAC
TOPMed
ClinGen
rs773567566
CA345144756
3 R>L No ClinGen
ExAC
gnomAD
rs773567566
CA1441476
3 R>P No ExAC
gnomAD
ClinGen
rs773567566
CA345144755
COSM905191
3 R>Q Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
rs748123791
CA1441473
4 T>A No ClinGen
ExAC
TOPMed
gnomAD
CA345144735
rs374675557
4 T>N No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs748123791
CA345144743
4 T>P No ExAC
TOPMed
gnomAD
ClinGen
CA1441472
rs374675557
4 T>S No ESP
ExAC
TOPMed
gnomAD
ClinGen
CA345144721
rs1422648667
5 K>E No gnomAD
ClinGen
rs1387025845
CA345144712
5 K>R No ClinGen
gnomAD
CA1441469
rs779875414
6 Q>L No ExAC
ClinGen
rs567472251
CA345144667
7 T>I No gnomAD
ClinGen
rs567472251
CA38748203
7 T>S No gnomAD
ClinGen
CA345144655
rs375918041
8 A>E No ExAC
TOPMed
gnomAD
ClinGen
CA1441468
rs114860054
8 A>T No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA1441467
rs375918041
8 A>V No ClinGen
ExAC
TOPMed
gnomAD
CA1441465
rs147766330
9 R>C No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs373549345
CA1441464
9 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA1441462
rs373549345
9 R>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs373549345
CA1441463
9 R>P No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA345144583
rs752078278
CA345144586
11 S>* No ClinGen
ExAC
TOPMed
gnomAD
rs1208768158
CA345144597
11 S>A No TOPMed
ClinGen
rs752078278
CA1441460
11 S>L No ClinGen
ExAC
TOPMed
gnomAD
CA38748173
rs1041442759
12 T>A No Ensembl
ClinGen
rs1410959088
CA345144570
12 T>M Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
CA1441456
rs765314078
13 G>A No ClinGen
ExAC
TOPMed
gnomAD
CA345144550
rs765314078
13 G>D No ClinGen
ExAC
TOPMed
gnomAD
rs1397772335
CA345144558
13 G>R No TOPMed
gnomAD
ClinGen
rs1397772335
CA345144561
13 G>S No TOPMed
gnomAD
ClinGen
CA1441454
rs567618899
14 G>D No ClinGen
1000Genomes
ExAC
gnomAD
CA1441452
rs369770019
15 K>N No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs547680085
CA1441453
15 K>Q No 1000Genomes
ExAC
TOPMed
gnomAD
ClinGen
CA345144487
rs1324149897
16 A>T No gnomAD
ClinGen
rs571515258
CA1441451
16 A>V No 1000Genomes
ExAC
TOPMed
gnomAD
ClinGen
rs151071964
CA1441449
17 P>L No ESP
ExAC
TOPMed
gnomAD
ClinGen
rs151071964
CA345144459
COSM3385874
17 P>Q pancreas [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
TOPMed
gnomAD
rs551314787
CA1441448
18 R>C No 1000Genomes
ExAC
gnomAD
ClinGen
rs756810829
CA1441447
18 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ExAC
TOPMed
gnomAD
ClinGen
NCI-TCGA
CA345144424
rs756810829
18 R>L No ClinGen
ExAC
TOPMed
gnomAD
rs756810829
CA38748135
18 R>P No ClinGen
ExAC
TOPMed
gnomAD
rs369767840
CA1441446
19 K>R No ESP
ExAC
TOPMed
gnomAD
ClinGen
CA1441445
rs777184854
20 Q>* No ExAC
ClinGen
rs375264894
CA38748116
22 A>T No ESP
TOPMed
gnomAD
ClinGen
CA1441444
rs755642778
22 A>V No ClinGen
ExAC
gnomAD
CA38748113
rs910077099
23 T>I No TOPMed
gnomAD
ClinGen
CA345144332
rs910077099
23 T>S No ClinGen
TOPMed
gnomAD
rs1574109655
CA345144308
24 K>R No ClinGen
Ensembl
TCGA novel 24 K>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA1441442
rs372401201
25 V>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA345144296
rs372401201
25 V>M No ESP
ExAC
TOPMed
gnomAD
ClinGen
rs758842988
CA1441441
26 A>V No ClinGen
ExAC
gnomAD
rs750781461
CA1441440
27 R>C No ExAC
TOPMed
gnomAD
ClinGen
COSM905190
CA1441439
rs765519082
27 R>H Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ExAC
TOPMed
gnomAD
ClinGen
cosmic curated
NCI-TCGA
CA345144232
rs765519082
27 R>P No ExAC
TOPMed
gnomAD
ClinGen
CA345144225
rs1275262455
28 K>E No ClinGen
TOPMed
gnomAD
CA345144200
rs1004441593
28 K>N No TOPMed
gnomAD
ClinGen
CA1441437
rs776883496
29 S>G No ClinGen
ExAC
gnomAD
rs531385963
CA1441433
30 A>P No 1000Genomes
ExAC
TOPMed
gnomAD
ClinGen
rs531385963
CA1441435
30 A>S No 1000Genomes
ExAC
TOPMed
gnomAD
ClinGen
rs531385963
CA1441434
30 A>T No 1000Genomes
ExAC
TOPMed
gnomAD
ClinGen
CA1441432
rs745685235
30 A>V No ExAC
TOPMed
gnomAD
ClinGen
rs377552351
CA1441429
31 P>L No ESP
ExAC
TOPMed
gnomAD
ClinGen
rs562257505
CA1441430
31 P>S Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1273784037
CA345144099
33 T>A Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No TOPMed
ClinGen
NCI-TCGA
rs200220156
CA345144088
33 T>I No 1000Genomes
ExAC
TOPMed
gnomAD
ClinGen
rs200220156
CA1441426
33 T>S No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA345144076
rs1190544502
34 G>D No ClinGen
gnomAD
rs750944754
CA345144068
35 G>C No ExAC
TOPMed
gnomAD
ClinGen
rs1201973529
CA345144064
35 G>D No ClinGen
gnomAD
COSM1209731
rs750944754
CA1441423
35 G>S large_intestine [Cosmic] No ExAC
TOPMed
gnomAD
ClinGen
cosmic curated
rs372584075
CA1441420
36 V>A No ESP
ExAC
TOPMed
gnomAD
ClinGen
CA1441421
rs372584075
36 V>E No ESP
ExAC
TOPMed
gnomAD
ClinGen
CA345144050
rs372584075
36 V>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA1441422
rs779185305
36 V>M No ExAC
gnomAD
ClinGen
TCGA novel 37 K>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA1441418
rs201151997
37 K>Q No 1000Genomes
ExAC
TOPMed
gnomAD
ClinGen
rs752725358
CA1441417
37 K>R No ExAC
ClinGen
rs774337671
CA1441415
38 K>M No ClinGen
ExAC
gnomAD
rs774337671
CA1441414
38 K>R No ExAC
gnomAD
ClinGen
rs1275672291
CA345143983
39 P>Q No gnomAD
ClinGen
rs1334201761
CA345143990
39 P>T No gnomAD
ClinGen
rs1177161942
CA345143964
40 H>R No gnomAD
ClinGen
CA1441412
rs762754764
40 H>Y No ExAC
TOPMed
gnomAD
ClinGen
CA1441410
rs769534943
41 R>C No ClinGen
ExAC
TOPMed
gnomAD
rs769534943
CA345143928
41 R>G No ClinGen
ExAC
TOPMed
gnomAD
rs769534943
CA345143931
41 R>S No ClinGen
ExAC
TOPMed
gnomAD
CA1441406
rs766963994
42 Y>* No ExAC
gnomAD
ClinGen
CA1441407
rs144390696
42 Y>C No 1000Genomes
ESP
ExAC
TOPMed
gnomAD
ClinGen
CA345143865
rs1484326215
43 R>G No TOPMed
gnomAD
ClinGen
CA345143854
rs1238300074
43 R>L No gnomAD
ClinGen
CA345143849
rs1435843313
44 P>A No gnomAD
ClinGen
CA345143847
rs1466119123
44 P>R No ClinGen
TOPMed
gnomAD
CA345143823
rs1358711210
45 G>D No gnomAD
ClinGen
rs746429747
CA1441404
45 G>R No ClinGen
ExAC
gnomAD
rs746429747
CA1441405
45 G>S Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
CA345143815
rs1358711210
45 G>V No ClinGen
gnomAD
CA1441402
COSM1209732
rs757564822
46 T>M Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ExAC
gnomAD
ClinGen
cosmic curated
NCI-TCGA
rs757564822
CA345143784
46 T>R No ClinGen
ExAC
gnomAD
CA345143760
rs777992092
47 V>L No ClinGen
ExAC
gnomAD
CA1441400
rs777992092
47 V>M Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs756376731
CA1441399
48 A>V No ClinGen
ExAC
gnomAD
rs752880989
CA1441398
49 L>F No ClinGen
ExAC
TOPMed
gnomAD
CA1441397
rs767647652
50 R>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA345143639
rs1161706855
51 E>G No ClinGen
gnomAD
rs201904037
CA1441396
53 R>H No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1177664534
CA345143588
53 R>S No gnomAD
ClinGen
rs751462450
CA1441395
54 R>G No ExAC
gnomAD
ClinGen
CA1441394
rs138699472
54 R>H No 1000Genomes
ESP
ExAC
TOPMed
gnomAD
ClinGen
CA38747850
rs867805240
55 Y>* No Ensembl
ClinGen
CA1441393
rs199974633
55 Y>C No 1000Genomes
ExAC
TOPMed
gnomAD
ClinGen
CA345143491
rs1205621529
56 Q>* No gnomAD
ClinGen
CA1441392
rs773014431
56 Q>R No ExAC
gnomAD
ClinGen
CA345143458
rs910118851
57 K>T No ClinGen
TOPMed
gnomAD
TCGA novel 57 K>missing Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs910118851
CA38747849
57 K>M No TOPMed
gnomAD
ClinGen
CA345143406
rs1321774460
58 S>C No gnomAD
ClinGen
rs1321774460
CA345143402
58 S>F No gnomAD
ClinGen
rs776419197
CA1441389
59 T>A No ExAC
gnomAD
ClinGen
rs768341466
CA1441388
59 T>I Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ExAC
gnomAD
ClinGen
NCI-TCGA
CA1441386
rs145767549
61 L>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs749735656
CA1441384
62 L>P No ExAC
gnomAD
ClinGen
CA345143305
rs2230656
63 I>M No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA1441380
rs201294185
64 R>C No 1000Genomes
ExAC
TOPMed
gnomAD
ClinGen
CA1441381
rs201294185
64 R>G No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA345143289
rs1350535396
64 R>L No gnomAD
ClinGen
CA38747794
rs777329716
65 K>T No ClinGen
Ensembl
rs755015645
CA345143250
CA1441378
66 L>F No ClinGen
ExAC
TOPMed
gnomAD
CA345143266
rs781330802
66 L>M No ClinGen
ExAC
TOPMed
gnomAD
rs781330802
CA1441379
66 L>V No ExAC
TOPMed
gnomAD
ClinGen
CA1441376
rs148883841
67 P>L No ESP
ExAC
gnomAD
ClinGen
CA1441377
rs201625757
67 P>S No ClinGen
1000Genomes
ExAC
gnomAD
CA1441374
CA345143213
rs144064739
68 F>L No 1000Genomes
ExAC
TOPMed
gnomAD
ClinGen
rs148655394
CA1441375
68 F>Y No 1000Genomes
ExAC
TOPMed
gnomAD
ClinGen
CA1441373
rs143341207
69 Q>* No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1215677963
CA345143202
69 Q>R No ClinGen
TOPMed
CA1441370
rs143639671
70 R>P No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA1441371
rs143639671
70 R>Q No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA1441372
rs761689329
70 R>W Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ExAC
gnomAD
ClinGen
NCI-TCGA
CA1441368
rs150702519
72 M>T No 1000Genomes
ESP
ExAC
TOPMed
gnomAD
ClinGen
rs1222575419
CA345143175
72 M>V No ClinGen
gnomAD
CA1441366
rs148579172
73 R>C No ESP
ExAC
TOPMed
ClinGen
rs148579172
CA1441365
73 R>G No ClinGen
ESP
ExAC
TOPMed
rs773691912
COSM281714
CA1441364
73 R>H Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ExAC
TOPMed
gnomAD
ClinGen
cosmic curated
NCI-TCGA
CA38747726
rs148579172
73 R>S No ClinGen
ESP
ExAC
TOPMed
CA1441361
rs781426750
75 I>M No ExAC
TOPMed
gnomAD
ClinGen
CA345143109
rs1558465152
75 I>V No Ensembl
ClinGen
rs369460992
CA1441360
76 A>P No ESP
ExAC
TOPMed
gnomAD
ClinGen
rs369460992
CA345143087
76 A>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs369460992
COSM3418867
CA345143090
76 A>T Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ESP
ExAC
TOPMed
gnomAD
ClinGen
cosmic curated
NCI-TCGA
rs747179869
CA1441359
76 A>V No ClinGen
ExAC
gnomAD
rs1574109345
CA345143072
77 Q>* No Ensembl
ClinGen
rs1000042512
CA38747710
77 Q>P No gnomAD
ClinGen
rs758405073
CA1441357
78 D>E No ClinGen
ExAC
gnomAD
rs780227110
CA1441358
78 D>N No ClinGen
ExAC
gnomAD
CA345143031
rs1348423079
79 F>I No ClinGen
TOPMed
rs750444463
CA1441356
79 F>S No ClinGen
ExAC
gnomAD
CA1441354
rs765210579
80 K>N No ClinGen
ExAC
TOPMed
gnomAD
CA1441353
rs753636972
81 T>I No ExAC
gnomAD
ClinGen
rs753636972
CA1441352
81 T>N No ExAC
gnomAD
ClinGen
rs1202634115
CA345142959
82 D>N No gnomAD
ClinGen
CA38747683
rs143162679
83 L>M No ESP
ExAC
TOPMed
ClinGen
CA38747678
rs143162679
83 L>V No ESP
ExAC
TOPMed
ClinGen
CA1441347
rs758908744
84 R>C No ClinGen
ExAC
CA345142885
rs1235890313
84 R>P No gnomAD
ClinGen
CA345142852
rs1313254665
86 Q>* No ClinGen
TOPMed
gnomAD
rs1482262254
CA345142804
88 S>L No ClinGen
TOPMed
CA345142815
rs1234923318
88 S>P No TOPMed
ClinGen
rs748538142
CA1441344
92 A>G No ClinGen
ExAC
gnomAD
rs1452175748
CA345142694
95 E>G No ClinGen
gnomAD
CA1441343
rs777033200
95 E>K No ClinGen
ExAC
gnomAD
CA1441342
rs768876038
96 A>S No ExAC
gnomAD
ClinGen
rs747322437
COSM1733939
CA1441341
96 A>V pancreas [Cosmic] No ExAC
gnomAD
ClinGen
cosmic curated
CA345142663
rs201439742
98 E>* No 1000Genomes
ExAC
gnomAD
ClinGen
rs201439742
CA1441338
98 E>Q No ClinGen
1000Genomes
ExAC
gnomAD
rs1179543240
CA345142656
98 E>V No TOPMed
ClinGen
rs1574109271
CA345142645
99 S>A No Ensembl
ClinGen
CA1441337
rs776386373
100 Y>* No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 100 Y>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA345142595
rs137880828
101 L>V No 1000Genomes
ESP
ExAC
TOPMed
gnomAD
ClinGen
CA1441335
rs779013955
102 V>G No ClinGen
ExAC
gnomAD
CA345142580
rs1390238114
102 V>M No ClinGen
gnomAD
CA345142517
rs1574109251
105 F>V No ClinGen
Ensembl
CA38747610
rs1052512820
106 E>D No ClinGen
TOPMed
CA38747612
rs868727723
106 E>G No Ensembl
ClinGen
CA345142469
rs1558465033
107 D>G No ClinGen
Ensembl
CA38747606
rs930162029
108 T>A No TOPMed
ClinGen
CA345142442
rs777690025
108 T>I No ClinGen
ExAC
gnomAD
CA1441331
rs777690025
108 T>S No ExAC
gnomAD
ClinGen
rs759075657
CA1441327
109 N>I No ExAC
gnomAD
ClinGen
CA345142415
rs1245345861
109 N>K No ClinGen
gnomAD
rs759075657
CA1441329
109 N>S No ExAC
gnomAD
ClinGen
CA1441328
rs759075657
109 N>T No ExAC
gnomAD
ClinGen
rs765855738
CA1441326
110 L>V No ExAC
TOPMed
gnomAD
ClinGen
rs1041180422
CA38747551
111 C>R No ClinGen
Ensembl
CA38747550
rs367745564
112 V>A No ClinGen
ESP
gnomAD
rs374791602
CA1441322
113 I>F No ESP
ExAC
gnomAD
ClinGen
CA1441321
rs769122987
113 I>M No ExAC
TOPMed
gnomAD
ClinGen
CA345142345
rs1215285009
113 I>T No TOPMed
ClinGen
rs374791602
CA1441323
113 I>V No ClinGen
ESP
ExAC
gnomAD
rs372972490
CA1441320
114 H>Y No ClinGen
ESP
ExAC
gnomAD
CA38747521
rs935358843
115 A>D No TOPMed
gnomAD
ClinGen
CA345142294
rs935358843
115 A>V No ClinGen
TOPMed
gnomAD
rs772146691
CA1441319
116 K>R No ClinGen
ExAC
TOPMed
gnomAD
rs772146691
CA1441318
116 K>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA38747518
COSM3689427
rs545672641
117 R>Q large_intestine Variant assessed as Somatic; impact. [Cosmic, NCI-TCGA] No 1000Genomes
ClinGen
cosmic curated
NCI-TCGA
COSM1997173
CA1441317
rs368511457
117 R>W central_nervous_system [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
TOPMed
gnomAD
rs1418217634
CA345142242
119 T>P No ClinGen
gnomAD
CA1441314
rs749296189
120 I>V No ExAC
gnomAD
ClinGen
CA1441312
rs755941555
121 M>R No ExAC
TOPMed
gnomAD
ClinGen
rs1420061280
CA345142220
121 M>V Variant assessed as Somatic; impact. [NCI-TCGA] No gnomAD
ClinGen
NCI-TCGA
rs1187813441
CA345142197
122 P>L No TOPMed
ClinGen
rs780917924
CA1441310
123 K>E No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 124 D>Y Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs751183313
CA1441308
126 Q>* No ClinGen
ExAC
TOPMed
gnomAD
rs375937549
CA1441307
126 Q>P No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA345142118
rs1332403307
128 A>V No ClinGen
TOPMed
rs1431559822
CA345142109
129 R>H Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
CA1441305
rs199657441
130 R>C No ExAC
TOPMed
gnomAD
ClinGen
rs146830002
CA1441304
130 R>H No ClinGen
ESP
ExAC
gnomAD
rs761134743
CA1441303
131 I>V No ClinGen
ExAC
gnomAD
CA1441302
rs775764888
132 R>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ExAC
gnomAD
ClinGen
NCI-TCGA
CA345142080
rs775764888
132 R>G No ClinGen
ExAC
gnomAD
CA345142076
rs1228332830
132 R>L No TOPMed
ClinGen
rs759900631
CA1441300
133 G>R No ClinGen
ExAC
TOPMed
gnomAD
CA345142057
rs1487311934
134 E>K No TOPMed
gnomAD
ClinGen
CA345142041
rs1277450211
135 R>Q No TOPMed
ClinGen
rs1163396027
CA345142028
136 A>V No gnomAD
ClinGen
rs774697896
CA1441299
137 A>W No ClinGen
ExAC
gnomAD

No associated diseases with Q16695

1 regional properties for Q16695

Type Name Position InterPro Accession
domain Histone H2A/H2B/H3 1 - 132 IPR007125

Functions

Description
EC Number
Subcellular Localization
  • Nucleus
  • Chromosome
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

5 GO annotations of cellular component

Name Definition
chromosome, telomeric region The end of a linear chromosome, required for the integrity and maintenance of the end. A chromosome telomere usually includes a region of telomerase-encoded repeats the length of which rarely exceeds 20 bp each and that permits the formation of a telomeric loop (T-loop). The telomeric repeat region is usually preceded by a sub-telomeric region that is gene-poor but rich in repetitive elements. Some telomeres only consist of the latter part (for eg. D. melanogaster telomeres).
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.
nucleoplasm That part of the nuclear content other than the chromosomes or the nucleolus.
nucleosome A complex comprised of DNA wound around a multisubunit core and associated proteins, which forms the primary packing unit of DNA into higher order structures.
nucleus A membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. In most cells, the nucleus contains all of the cell's chromosomes except the organellar chromosomes, and is the site of RNA synthesis and processing. In some species, or in specialized cell types, RNA metabolism or DNA replication may be absent.

3 GO annotations of molecular function

Name Definition
DNA binding Any molecular function by which a gene product interacts selectively and non-covalently with DNA (deoxyribonucleic acid).
protein heterodimerization activity Binding to a nonidentical protein to form a heterodimer.
structural constituent of chromatin The action of a molecule that contributes to the structural integrity of chromatin.

1 GO annotations of biological process

Name Definition
nucleosome assembly The aggregation, arrangement and bonding together of a nucleosome, the beadlike structural units of eukaryotic chromatin composed of histones and DNA.

35 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
P68428 Histone H3.2 Triticum aestivum (Wheat) PR
Q5E9F8 H3-3B Histone H3.3 Bos taurus (Bovine) PR
P68432 Histone H3.1 Bos taurus (Bovine) PR
P84227 Histone H3.2 Bos taurus (Bovine) PR
P84247 H3-X Histone H3.3 Gallus gallus (Chicken) PR
P84229 H3-VIII Histone H3.2 Gallus gallus (Chicken) PR
P02299 His3 Histone H3 Drosophila melanogaster (Fruit fly) PR
Q71H73 Histone H3.3 Vitis vinifera (Grape) PR
P68431 H3C12 Histone H3.1 Homo sapiens (Human) PR
P84243 H3-3B Histone H3.3 Homo sapiens (Human) PR
Q71DI3 H3C13 Histone H3.2 Homo sapiens (Human) PR
P69246 H3C4 Histone H3.2 Zea mays (Maize) PR
P84228 H3c15 Histone H3.2 Mus musculus (Mouse) PR
P68433 H3c11 Histone H3.1 Mus musculus (Mouse) PR
P84244 H3-3b Histone H3.3 Mus musculus (Mouse) PR
Q71LE2 H3-3A Histone H3.3 Sus scrofa (Pig) PR
P84245 H3-3b Histone H3.3 Rattus norvegicus (Rat) PR
O35799 Hfe Hereditary hemochromatosis protein homolog Rattus norvegicus (Rat) PR
Q6LED0 Histone H3.1 Rattus norvegicus (Rat) PR
Q0JCT1 H3 Histone H3.3 Oryza sativa subsp japonica (Rice) PR
Q2RAD9 H3R-21 Histone H3.2 Oryza sativa subsp japonica (Rice) PR
Q27490 his-70 Histone H3.3-like type 1 Caenorhabditis elegans PR
Q10453 his-71 Histone H3.3 type 1 Caenorhabditis elegans PR
Q27532 his-74 Histone H3.3-like type 2 Caenorhabditis elegans PR
P08898 his-2 Histone H3 Caenorhabditis elegans PR
Q9FX60 At1g13370 Histone H3-like 1 Arabidopsis thaliana (Mouse-ear cress) PR
Q9FXI7 MGH3 Histone H3-like 2 Arabidopsis thaliana (Mouse-ear cress) PR
Q9FKQ3 At5g65350 Histone H3-like 5 Arabidopsis thaliana (Mouse-ear cress) PR
P59226 HTR2 Histone H3.1 Arabidopsis thaliana (Mouse-ear cress) PR
Q9LR02 At1g75600 Histone H3-like 3 Arabidopsis thaliana (Mouse-ear cress) PR
P59169 HTR4 Histone H3.3 Arabidopsis thaliana (Mouse-ear cress) PR
Q6P823 TGas113e22.1 Histone H3.3 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
Q28D37 TGas081o10.1 Histone H3.2 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
Q6PI20 h3f3a Histone H3.3 Danio rerio (Zebrafish) (Brachydanio rerio) PR
Q4QRF4 zgc:113984; Histone H3.2 Danio rerio (Zebrafish) (Brachydanio rerio) PR
10 20 30 40 50 60
MARTKQTARK STGGKAPRKQ LATKVARKSA PATGGVKKPH RYRPGTVALR EIRRYQKSTE
70 80 90 100 110 120
LLIRKLPFQR LMREIAQDFK TDLRFQSSAV MALQEACESY LVGLFEDTNL CVIHAKRVTI
130
MPKDIQLARR IRGERA