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

3 structures for Q9UN19

Entry ID Method Resolution Chain Position Source
1FAO X-ray 180 A A 148-273 PDB
1FB8 X-ray 240 A A 148-273 PDB
AF-Q9UN19-F1 Predicted AlphaFoldDB

165 variants for Q9UN19

Variant ID(s) Position Change Description Diseaes Association Provenance
rs1419135132
CA357556146
4 A>V No ClinGen
TOPMed
CA357556147
rs1322733149
5 E>K No ClinGen
gnomAD
TCGA novel 8 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3022788
rs757550910
8 E>Q No ClinGen
ExAC
gnomAD
rs781263514
CA3022790
10 K>E No ClinGen
ExAC
gnomAD
rs1316260255
CA357556362
10 K>N Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs750517647
CA3022791
11 M>I No ClinGen
ExAC
gnomAD
TCGA novel 11 M>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA357556405
rs1266285786
12 S>T No ClinGen
TOPMed
gnomAD
rs192454033
CA3022794
15 D>N No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA102673222
rs924134918
15 D>V No ClinGen
TOPMed
rs1488938032
CA357556549
16 P>T No ClinGen
gnomAD
CA357556701
rs1260351059
21 S>N No ClinGen
gnomAD
rs778726455
CA3022796
21 S>R No ClinGen
ExAC
gnomAD
rs747880443
CA3022797
23 S>A No ClinGen
ExAC
gnomAD
CA102673234
rs373752102
24 D>N No ClinGen
TOPMed
gnomAD
rs772675090
CA3022799
25 G>R No ClinGen
ExAC
gnomAD
rs1361063932
CA357556947
27 A>G No ClinGen
gnomAD
rs760245627
CA3022800
28 E>K No ClinGen
ExAC
gnomAD
rs900592526
CA102673242
32 D>N No ClinGen
TOPMed
CA357560024
rs1291040868
35 W>* No ClinGen
TOPMed
gnomAD
CA357560033
rs1291040868
35 W>C No ClinGen
TOPMed
gnomAD
TCGA novel 37 H>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA357560110
rs1314674975
38 G>D No ClinGen
gnomAD
rs770680155
CA3022818
38 G>S No ClinGen
ExAC
TOPMed
gnomAD
rs969041709
CA102681032
40 L>F No ClinGen
TOPMed
CA3022819
rs776332284
42 R>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
CA357560211
rs1214491721
43 H>Y No ClinGen
TOPMed
CA3022820
rs200313632
44 A>T No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA357560247
rs1316900852
44 A>V No ClinGen
gnomAD
rs554960188
CA3022825
55 D>E No ClinGen
ExAC
TOPMed
gnomAD
rs1469469055
CA357560468
55 D>N No ClinGen
gnomAD
CA102681059
rs866782436
56 G>D No ClinGen
Ensembl
CA3022826
COSM225549
rs760935963
56 G>S NS [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
rs1238421501
CA357560497
57 S>R No ClinGen
gnomAD
CA357560591
rs1578356067
62 D>G No ClinGen
Ensembl
rs1037696561
CA102681063
62 D>H No ClinGen
TOPMed
rs371733623
CA3022827
63 S>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1387030622
CA357560672
65 E>D No ClinGen
gnomAD
rs749215963
CA102681064
66 T>P No ClinGen
Ensembl
rs920634897
CA102681067
67 T>I No ClinGen
TOPMed
rs754986506
CA3022829
68 G>R No ClinGen
ExAC
TOPMed
gnomAD
rs752528304
CA3022831
72 L>V Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs746781776
CA3022834
73 S>C No ClinGen
ExAC
TOPMed
gnomAD
CA357500423
rs1200475300
75 R>S No ClinGen
Ensembl
CA3022850
rs531841086
76 A>S No ClinGen
1000Genomes
ExAC
gnomAD
rs267599964
CA102613668
83 F>C No ClinGen
Ensembl
rs541741416
CA102613670
84 H>L No ClinGen
ExAC
gnomAD
rs541741416
CA3022851
84 H>R No ClinGen
ExAC
gnomAD
TCGA novel 87 Y>F Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA357500588
rs1212400726
90 Y>C No ClinGen
gnomAD
rs757057345
CA3022852
90 Y>H No ClinGen
ExAC
gnomAD
CA102613698
rs937899470
91 S>* No ClinGen
TOPMed
gnomAD
rs1322025255
CA357500626
93 K>E No ClinGen
gnomAD
TCGA novel 95 G>D Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA357500700
rs1223574998
97 N>S No ClinGen
TOPMed
gnomAD
rs763855611
CA357500724
98 E>D No ClinGen
ExAC
gnomAD
TCGA novel 101 S>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3022855
rs559809943
102 L>V No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 110 A>* Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1166311370
CA357500928
111 N>Y No ClinGen
gnomAD
rs748817839
CA3022857
113 P>A No ClinGen
ExAC
gnomAD
CA357500960
rs748817839
113 P>S No ClinGen
ExAC
gnomAD
rs1364232361
CA357500999
116 G>R No ClinGen
gnomAD
rs747389030
CA3022860
119 T>I No ClinGen
ExAC
gnomAD
rs746234384
CA3022883
120 G>D No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 125 L>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1443109256
CA357504825
127 H>Y No ClinGen
gnomAD
CA800771110
rs1227177668
129 Y>* No ClinGen
TOPMed
CA3022889
rs761887882
130 P>A No ClinGen
ExAC
gnomAD
rs767547987
CA3022890
131 R>* No ClinGen
ExAC
gnomAD
CA357504944
rs1304171618
132 K>Q No ClinGen
TOPMed
CA3022891
rs750309314
133 V>M No ClinGen
ExAC
gnomAD
rs760451809
CA3022892
134 E>K No ClinGen
ExAC
gnomAD
CA357505095
COSM1633384
rs1402230230
COSM1633385
138 I>V liver [Cosmic] No ClinGen
cosmic curated
gnomAD
rs1399985064
CA357505186
140 E>G No ClinGen
TOPMed
rs908547761
CA102623903
141 S>F Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs753481523
CA3022894
142 V>I No ClinGen
ExAC
gnomAD
CA3022896
rs376041630
143 R>Q No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs548601611
CA3022895
143 R>W No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA357505255
rs1333878672
144 V>I No ClinGen
gnomAD
rs1238193992
CA357505329
146 T>I No ClinGen
gnomAD
COSM1049463
rs752181928
COSM1049462
CA3022897
147 A>T Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
rs1345742408
CA357505422
150 T>I No ClinGen
gnomAD
CA357505471
rs1416262925
153 T>K No ClinGen
TOPMed
rs1225437924
CA357505522
155 D>V No ClinGen
gnomAD
rs901853231
CA357505545
156 D>E No ClinGen
gnomAD
CA102623923
rs1014853943
156 D>V No ClinGen
gnomAD
CA357505550
rs1199627336
157 L>V No ClinGen
gnomAD
CA357505610
rs1181646090
COSM1049465
161 A>S Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
CA357505621
rs1481129131
163 S>P No ClinGen
gnomAD
rs368943931
CA3022912
165 G>A No ClinGen
ESP
ExAC
TOPMed
gnomAD
COSM1049466
rs368943931
COSM1049467
CA102629869
165 G>D endometrium [Cosmic] No ClinGen
cosmic curated
ESP
ExAC
TOPMed
gnomAD
rs368943931
CA357507323
165 G>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA357507347
rs1422617710
169 G>S No ClinGen
gnomAD
rs747022017
CA102629886
171 L>F No ClinGen
Ensembl
CA102629891
rs747022017
171 L>I No ClinGen
Ensembl
rs1270781082
CA357507366
172 T>A Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA357507384
rs1302509845
174 Q>L No ClinGen
gnomAD
rs759283422
CA3022914
175 G>* No ClinGen
ExAC
gnomAD
rs1400705615
CA357507399
176 G>V No ClinGen
gnomAD
CA357507406
rs1297979130
177 L>P No ClinGen
gnomAD
CA357507412
rs1227111285
178 V>I No ClinGen
TOPMed
gnomAD
CA357507414
rs1227111285
178 V>L No ClinGen
TOPMed
gnomAD
CA102630665
rs964769892
180 T>S No ClinGen
Ensembl
CA357507543
rs1450903455
186 F>L No ClinGen
TOPMed
gnomAD
CA3022939
rs751007881
187 T>I No ClinGen
ExAC
gnomAD
TCGA novel 190 R>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1052230460
CA102630674
193 L>V No ClinGen
TOPMed
rs892325298
CA357507593
194 K>R No ClinGen
TOPMed
gnomAD
CA102630675
rs892325298
194 K>T No ClinGen
TOPMed
gnomAD
CA357507617
rs1238509248
197 K>R No ClinGen
gnomAD
CA3022942
rs754233433
198 D>E No ClinGen
ExAC
TOPMed
gnomAD
CA357507625
rs1331078282
198 D>G No ClinGen
TOPMed
CA102630681
rs1022656109
200 M>T No ClinGen
TOPMed
CA357507659
rs1223496061
201 S>L No ClinGen
TOPMed
CA3022964
rs753089835
202 P>L No ClinGen
ExAC
gnomAD
rs1043952547
CA102631105
203 E>V No ClinGen
TOPMed
gnomAD
rs867913952
CA357507678
204 P>L Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs867913952
CA102631107
204 P>Q No ClinGen
gnomAD
CA3022966
rs201164049
205 I>V No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1020531964
CA102631119
206 R>Q Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs1272082115
CA357507702
209 D>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs1560709898
CA357507710
210 L>V No ClinGen
Ensembl
TCGA novel 212 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 217 Q>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA357507768
rs3737484
218 F>L No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA357507763
rs1392853925
218 F>L No ClinGen
TOPMed
rs745769238
CA3022970
219 D>N Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA3022972
rs769693769
221 S>P No ClinGen
ExAC
gnomAD
rs1383892303
CA357508928
233 P>S Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs764393680
CA3022989
235 R>G No ClinGen
ExAC
gnomAD
CA3022990
rs751687566
236 T>I No ClinGen
ExAC
gnomAD
CA357509046
rs1560711472
237 F>S No ClinGen
Ensembl
CA357509102
rs1398470642
238 Y>C No ClinGen
gnomAD
rs1035507327
CA102632416
241 A>G No ClinGen
Ensembl
CA357509181
rs1477410465
241 A>T No ClinGen
TOPMed
CA357509255
rs756108686
244 G>* No ClinGen
ExAC
TOPMed
gnomAD
CA3022994
rs756108686
CA357509252
244 G>R No ClinGen
ExAC
TOPMed
gnomAD
CA357509391
rs1454350205
250 W>L No ClinGen
gnomAD
CA357509400
rs1334504272
251 I>V No ClinGen
gnomAD
CA102632454
rs746077539
254 L>V No ClinGen
Ensembl
rs779897890
CA3022995
255 R>C No ClinGen
ExAC
gnomAD
CA3022996
rs749093298
255 R>H No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 255 R>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA357509498
rs1281216241
256 W>* No ClinGen
gnomAD
CA357509699
rs1243107994
260 Q>* No ClinGen
gnomAD
CA102633992
rs867048585
260 Q>H No ClinGen
Ensembl
TCGA novel 261 I>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA3023041
rs187147584
263 K>R No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA3023042
rs780620801
264 Q>E No ClinGen
ExAC
TOPMed
gnomAD
rs924399278
CA102634013
265 L>I No ClinGen
TOPMed
gnomAD
CA357509739
rs1259247322
266 N>Y No ClinGen
TOPMed
gnomAD
rs745376074
CA3023043
269 E>D No ClinGen
ExAC
gnomAD
rs879122474
CA102634014
269 E>Q No ClinGen
Ensembl
rs942470925
CA102634015
270 G>S No ClinGen
Ensembl
rs769044015
CA3023044
271 T>M No ClinGen
ExAC
TOPMed
gnomAD
CA3023046
rs200809136
273 R>* No ClinGen
ExAC
TOPMed
gnomAD
CA3023048
rs371219607
273 R>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA3023047
rs371219607
273 R>Q No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1249025727
CA357509791
275 R>Q No ClinGen
TOPMed
CA3023049
rs760935827
275 R>W No ClinGen
ExAC
TOPMed
gnomAD
CA357509797
rs1386810500
276 S>L No ClinGen
TOPMed
gnomAD
rs1231647342
CA357509822
279 F>L No ClinGen
TOPMed
rs759595702
CA3023052
280 K>N No ClinGen
ExAC
gnomAD

No associated diseases with Q9UN19

3 regional properties for Q9UN19

Type Name Position InterPro Accession
domain SH2 domain 33 - 129 IPR000980
domain Pleckstrin homology domain 164 - 261 IPR001849
domain DAPP1, SH2 domain 28 - 119 IPR035843

Functions

Description
EC Number
Subcellular Localization
  • Cytoplasm
  • Membrane ; Peripheral membrane protein
  • Membrane-associated after cell stimulation leading to its translocation
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

2 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.
plasma membrane The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins.

3 GO annotations of molecular function

Name Definition
phosphatidylinositol-3,4,5-trisphosphate binding Binding to phosphatidylinositol-3,4,5-trisphosphate, a derivative of phosphatidylinositol in which the inositol ring is phosphorylated at the 3', 4' and 5' positions.
phosphatidylinositol-3,4-bisphosphate binding Binding to phosphatidylinositol-3,4-bisphosphate, a derivative of phosphatidylinositol in which the inositol ring is phosphorylated at the 3' and 4' positions.
phospholipid binding Binding to a phospholipid, a class of lipids containing phosphoric acid as a mono- or diester.

2 GO annotations of biological process

Name Definition
protein dephosphorylation The process of removing one or more phosphoric residues from a protein.
signal transduction The cellular process in which a signal is conveyed to trigger a change in the activity or state of a cell. Signal transduction begins with reception of a signal (e.g. a ligand binding to a receptor or receptor activation by a stimulus such as light), or for signal transduction in the absence of ligand, signal-withdrawal or the activity of a constitutively active receptor. Signal transduction ends with regulation of a downstream cellular process, e.g. regulation of transcription or regulation of a metabolic process. Signal transduction covers signaling from receptors located on the surface of the cell and signaling via molecules located within the cell. For signaling between cells, signal transduction is restricted to events at and within the receiving cell.

11 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
A4FUB7 GIN1 Gypsy retrotransposon integrase-like protein 1 Bos taurus (Bovine) PR
Q6ZNG9 KRBA2 KRAB-A domain-containing protein 2 Homo sapiens (Human) PR
Q9P2P1 NYNRIN Protein NYNRIN Homo sapiens (Human) PR
Q6R2W3 ZBED9 SCAN domain-containing protein 3 Homo sapiens (Human) PR
Q9QXT1 Dapp1 Dual adapter for phosphotyrosine and 3-phosphotyrosine and 3-phosphoinositide Mus musculus (Mouse) PR
Q94KB1 MLO14 MLO-like protein 14 Arabidopsis thaliana (Mouse-ear cress) PR
O80580 MLO15 MLO-like protein 15 Arabidopsis thaliana (Mouse-ear cress) PR
Q9SMP1 XTH11 Probable xyloglucan endotransglucosylase/hydrolase protein 11 Arabidopsis thaliana (Mouse-ear cress) PR
O49621 MLO1 MLO-like protein 1 Arabidopsis thaliana (Mouse-ear cress) PR
Q9FK75 At5g45670 GDSL esterase/lipase At5g45670 Arabidopsis thaliana (Mouse-ear cress) PR
Q9FI00 MLO11 MLO-like protein 11 Arabidopsis thaliana (Mouse-ear cress) PR
10 20 30 40 50 60
MGRAELLEGK MSTQDPSDLW SRSDGEAELL QDLGWYHGNL TRHAAEALLL SNGCDGSYLL
70 80 90 100 110 120
RDSNETTGLY SLSVRAKDSV KHFHVEYTGY SFKFGFNEFS SLKDFVKHFA NQPLIGSETG
130 140 150 160 170 180
TLMVLKHPYP RKVEEPSIYE SVRVHTAMQT GRTEDDLVPT APSLGTKEGY LTKQGGLVKT
190 200 210 220 230 240
WKTRWFTLHR NELKYFKDQM SPEPIRILDL TECSAVQFDY SQERVNCFCL VFPFRTFYLC
250 260 270
AKTGVEADEW IKILRWKLSQ IRKQLNQGEG TIRSRSFIFK