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 Q9UD71

Entry ID Method Resolution Chain Position Source
AF-Q9UD71-F1 Predicted AlphaFoldDB

157 variants for Q9UD71

Variant ID(s) Position Change Description Diseaes Association Provenance
CA290410891
rs952716568
4 K>E No ClinGen
Ensembl
CA399262701
rs547648169
6 R>H No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs547648169
CA8531939
6 R>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs761179656
CA8531940
7 K>R No ClinGen
ExAC
TOPMed
gnomAD
rs1161651631
CA399262754
9 I>L No ClinGen
gnomAD
CA399262780
rs1371861232
10 Q>P No ClinGen
gnomAD
rs1309734047
CA399262812
11 F>L Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
rs1415111106
CA399262806
11 F>S No ClinGen
TOPMed
gnomAD
rs1462084175
CA399262830
12 S>L No ClinGen
gnomAD
CA8531941
rs766668979
14 P>L No ClinGen
ExAC
gnomAD
CA290410897
rs961996489
16 P>L No ClinGen
Ensembl
CA290410896
rs1016171854
16 P>S No ClinGen
Ensembl
CA399262905
rs1398117032
17 P>L No ClinGen
gnomAD
rs1337810833
CA399262916
18 S>G No ClinGen
gnomAD
rs971883980
CA399262932
CA290410899
18 S>R No ClinGen
TOPMed
gnomAD
CA399262954
rs1244407066
19 Q>R No ClinGen
gnomAD
rs779075907
CA8531944
21 D>E No ClinGen
ExAC
TOPMed
gnomAD
CA8531943
rs755222458
21 D>G No ClinGen
ExAC
gnomAD
TCGA novel 23 R>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA399263136
rs1243509329
26 E>D No ClinGen
gnomAD
rs1460757564
CA399263141
27 M>L No ClinGen
gnomAD
CA8531963
rs367543179
29 R>L Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
CA225905
rs367543179
RCV000084768
29 R>Q No ClinGen
ClinVar
ESP
ExAC
TOPMed
dbSNP
gnomAD
rs1304514528
CA399263646
29 R>W No ClinGen
TOPMed
rs756069251
CA8531964
30 R>C No ClinGen
ExAC
CA8531965
rs780007110
30 R>H No ClinGen
ExAC
TOPMed
gnomAD
rs1468522759
CA399263714
31 R>M No ClinGen
gnomAD
TCGA novel 32 R>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs971270763
CA290411301
33 P>L No ClinGen
TOPMed
gnomAD
CA399263784
rs1346245001
34 T>M No ClinGen
gnomAD
rs1287695645
CA399263849
36 A>D No ClinGen
gnomAD
CA8531967
rs368811507
40 R>Q No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1405677322
CA399263937
40 R>W Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs778787065
CA8531968
42 S>L No ClinGen
ExAC
gnomAD
rs775936429
CA399264438
50 E>D No ClinGen
ExAC
gnomAD
CA8531993
rs201594054
51 A>D No ClinGen
ExAC
TOPMed
gnomAD
rs201594054
CA399264496
51 A>G No ClinGen
ExAC
TOPMed
gnomAD
rs201594054
CA399264478
51 A>V No ClinGen
ExAC
TOPMed
gnomAD
CA399264502
rs1337240564
52 S>T No ClinGen
TOPMed
CA399264521
rs1434278389
52 S>Y No ClinGen
TOPMed
rs1567847557
CA399264536
53 P>A No ClinGen
Ensembl
rs145932715
CA399264572
54 H>D No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs145932715
CA8531995
54 H>N No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1383457396 54 H>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA290411400
rs896774899
55 Q>E No ClinGen
Ensembl
CA399264903
rs1201825976
56 R>T No ClinGen
TOPMed
gnomAD
TCGA novel 57 A>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA8532018
rs774523933
61 G>R No ClinGen
ExAC
gnomAD
CA399265113
rs1470088091
63 H>R No ClinGen
gnomAD
CA8532019
rs377425724
64 L>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA399265227
rs1399902677
66 S>A No ClinGen
gnomAD
COSM978639
rs200974893
CA8532020
66 S>L Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
CA399265373
rs1159938127
70 N>Y No ClinGen
TOPMed
gnomAD
CA8532022
rs199925027
71 P>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs140199436
CA290411536
72 C>R No ClinGen
ESP
rs1032368917
CA290411538
72 C>Y No ClinGen
TOPMed
CA399265626
rs1284755691
75 T>I No ClinGen
gnomAD
CA290411542
rs922146710
78 S>L No ClinGen
TOPMed
gnomAD
CA8532045
rs751406867
81 A>G No ClinGen
ExAC
gnomAD
rs1392259387
CA399267686
82 V>M No ClinGen
gnomAD
CA8532047
rs767247081
84 R>C No ClinGen
ExAC
TOPMed
gnomAD
rs139360619
CA8532049
COSM705328
84 R>H lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs139360619
CA8532050
84 R>L No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA8532048
rs767247081
84 R>S No ClinGen
ExAC
TOPMed
gnomAD
rs1253254924
CA399267979
93 I>L No ClinGen
gnomAD
rs1253254924
CA399267981
93 I>V No ClinGen
gnomAD
CA399268069
rs1597781172
95 N>S No ClinGen
Ensembl
TCGA novel 97 N>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1237330238
CA399268263
100 Q>H No ClinGen
gnomAD
CA8532055
rs758721684
101 A>V No ClinGen
ExAC
TOPMed
gnomAD
CA399268305
rs1185321761
103 E>K No ClinGen
gnomAD
CA8532056
rs778216588
104 E>G No ClinGen
ExAC
gnomAD
CA399268421
rs1162095494
105 E>D No ClinGen
gnomAD
rs747247652
CA8532057
105 E>K No ClinGen
ExAC
gnomAD
CA399268512
rs1374379241
107 E>G No ClinGen
gnomAD
rs1597781212
CA399268576
109 G>R No ClinGen
Ensembl
CA399268603
rs1167030170
109 G>V No ClinGen
gnomAD
CA8532059
rs776915939
110 E>D No ClinGen
ExAC
gnomAD
CA399268678
rs1262166630
112 R>P No ClinGen
TOPMed
rs1262166630
CA399268675
112 R>Q No ClinGen
TOPMed
rs934858687
CA290413032
112 R>W No ClinGen
TOPMed
rs1239288175
CA399268695
113 E>K No ClinGen
TOPMed
CA8532060
rs745902423
116 Y>N No ClinGen
ExAC
gnomAD
rs1394300459
CA399268790
119 E>K No ClinGen
gnomAD
CA399268865
rs1297838615
121 D>G No ClinGen
gnomAD
CA8532063
rs768685523
122 E>K No ClinGen
ExAC
gnomAD
CA399268944
rs1226964800
123 E>D No ClinGen
gnomAD
rs922722288
CA290413046
125 E>K No ClinGen
Ensembl
rs144685420
CA8532067
126 E>D No ClinGen
1000Genomes
ESP
ExAC
TOPMed
CA8532065
rs774173341
126 E>G No ClinGen
ExAC
TOPMed
gnomAD
CA8532068
rs767316801
127 D>E No ClinGen
ExAC
TOPMed
gnomAD
CA399269043
rs1567849504
128 D>E No ClinGen
Ensembl
rs747625780
CA290413057
129 E>D No ClinGen
ExAC
gnomAD
TCGA novel 131 E>* Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs765988806
CA8532074
131 E>K No ClinGen
ExAC
gnomAD
CA8532076
rs754471109
133 E>A No ClinGen
ExAC
TOPMed
gnomAD
CA399269155
rs1263214759
133 E>K No ClinGen
gnomAD
TCGA novel 138 Q>H Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA399269345
rs1421049807
139 A>D No ClinGen
gnomAD
CA8532078
rs753149836
142 L>P No ClinGen
ExAC
gnomAD
TCGA novel 143 K>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA290413077
rs888452883
144 V>L No ClinGen
Ensembl
rs371198090
CA8532080
145 I>F No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs180955049
CA8532081
146 R>K No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1381740448
CA399269574
147 Q>H No ClinGen
gnomAD
rs757592685
CA8532082
148 S>Y No ClinGen
ExAC
TOPMed
gnomAD
CA8532104
rs756349197
149 A>G No ClinGen
ExAC
gnomAD
CA399269594
rs1171470511
149 A>T No ClinGen
gnomAD
rs780069107
CA8532105
151 Q>R No ClinGen
ExAC
gnomAD
rs1179319652
CA399270899
152 K>Q No ClinGen
gnomAD
CA399270957
rs1597782674
153 T>A No ClinGen
Ensembl
rs946950591
CA290413576
153 T>K No ClinGen
TOPMed
gnomAD
CA8532107
rs142405059
156 G>S No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1597782695
CA399271088
159 L>P No ClinGen
Ensembl
CA290413578
rs923563706
160 E>G No ClinGen
TOPMed
rs867953055
CA290413588
164 E>K No ClinGen
Ensembl
CA8532110
COSM2156691
rs367543181
165 R>C central_nervous_system [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
CA399271247
rs1433950150
165 R>H No ClinGen
gnomAD
RCV000084770
rs367543181
CA225909
165 R>S No ClinGen
ClinVar
ExAC
TOPMed
dbSNP
gnomAD
CA8532112
rs759168684
167 P>H No ClinGen
ExAC
gnomAD
rs75805989
CA8532111
167 P>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA290413595
rs75805989
167 P>T No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA8532113
rs201468603
168 P>A No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs201468603
CA8532115
168 P>S No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs201468603
CA8532114
168 P>T No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1307049040
CA399271330
169 L>V No ClinGen
gnomAD
CA399271364
rs1360953726
170 D>E No ClinGen
gnomAD
rs142312063
CA290413612
173 E>* No ClinGen
ESP
TOPMed
gnomAD
rs762341431
CA8532118
173 E>D No ClinGen
ExAC
gnomAD
rs142312063
CA290413609
173 E>K No ClinGen
ESP
TOPMed
gnomAD
rs767783990
CA8532119
174 R>K No ClinGen
ExAC
gnomAD
rs112102104
CA8532120
176 G>E No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA8532121
rs756335286
177 G>S No ClinGen
ExAC
gnomAD
rs1238949710
CA399271536
179 E>K No ClinGen
TOPMed
rs1238949710
CA399271540
179 E>Q No ClinGen
TOPMed
rs754012099
CA8532123
180 D>G No ClinGen
ExAC
TOPMed
gnomAD
CA399271578
rs754012099
180 D>V No ClinGen
ExAC
TOPMed
gnomAD
CA399271631
rs778899903
181 Q>H No ClinGen
ExAC
gnomAD
rs746964011
CA8532126
184 D>N No ClinGen
ExAC
TOPMed
gnomAD
CA399271787
rs1171477074
186 A>E No ClinGen
TOPMed
gnomAD
CA290413631
rs960744652
187 L>V No ClinGen
gnomAD
CA399272056
rs1210795207
191 G>A No ClinGen
TOPMed
CA8532142
rs755137721
194 P>S No ClinGen
ExAC
TOPMed
gnomAD
CA290413677
rs562428995
195 Q>R No ClinGen
Ensembl
CA8532143
COSM4129947
rs35797948
196 R>H thyroid [Cosmic] No ClinGen
cosmic curated
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs910863560
CA290413681
197 P>A No ClinGen
TOPMed
CA290413692
rs79497069
198 S>F No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA399272297
rs1356907425
198 S>T No ClinGen
gnomAD
rs79497069
RCV000955271
CA8532144
198 S>Y No ClinGen
ClinVar
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
rs757180713
CA8532145
199 P>H No ClinGen
ExAC
gnomAD
rs757180713
CA290413698
199 P>L No ClinGen
ExAC
gnomAD
rs535690693
CA8532146
200 S>A No ClinGen
1000Genomes
ExAC
gnomAD
rs1217122660
CA399272347
200 S>C No ClinGen
gnomAD
CA8532148
rs745743199
203 G>R No ClinGen
ExAC
gnomAD
rs745743199
CA8532147
203 G>S No ClinGen
ExAC
gnomAD
rs1388739789
CA399272512
204 T>I No ClinGen
TOPMed
rs779924792
CA8532149
205 T>Q No ClinGen
ExAC
gnomAD

No associated diseases with Q9UD71

No regional properties for Q9UD71

Type Name Position InterPro Accession
No domain, repeats, and functional sites for Q9UD71

Functions

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

4 GO annotations of cellular component

Name Definition
cytoplasm The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures.
cytosol The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.
neuronal cell body The portion of a neuron that includes the nucleus, but excludes cell projections such as axons and dendrites.
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.

4 GO annotations of molecular function

Name Definition
cAMP-dependent protein kinase inhibitor activity Binds to and stops, prevents or reduces the activity of a cAMP-dependent protein kinase.
protein kinase inhibitor activity Binds to and stops, prevents or reduces the activity of a protein kinase, an enzyme which phosphorylates a protein.
protein phosphatase inhibitor activity Binds to and stops, prevents or reduces the activity of a protein phosphatase, an enzyme that hydrolyzes phosphate groups from phosphorylated proteins.
protein phosphatase regulator activity Binds to and modulates the activity of a protein phosphatase, an enzyme which catalyzes of the removal of a phosphate group from a protein substrate molecule.

11 GO annotations of biological process

Name Definition
behavioral response to cocaine Any process that results in a change in the behavior of an organism as a result of a cocaine stimulus.
cellular response to cocaine Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a cocaine stimulus. Cocaine is a crystalline alkaloid obtained from the leaves of the coca plant.
DNA-templated transcription The synthesis of an RNA transcript from a DNA template.
intracellular signal transduction The process in which a signal is passed on to downstream components within the cell, which become activated themselves to further propagate the signal and finally trigger a change in the function or state of the cell.
locomotory behavior The specific movement from place to place of an organism in response to external or internal stimuli. Locomotion of a whole organism in a manner dependent upon some combination of that organism's internal state and external conditions.
negative regulation of female receptivity Any process that stops, prevents or reduces the receptiveness of a female to male advances.
negative regulation of phosphoprotein phosphatase activity Any process that stops or reduces the activity of a phosphoprotein phosphatase.
response to amphetamine Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an amphetamine stimulus. Amphetamines consist of a group of compounds related to alpha-methylphenethylamine.
response to morphine Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a morphine stimulus. Morphine is an opioid alkaloid, isolated from opium, with a complex ring structure.
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.
visual learning Any process in an organism in which a change in behavior of an individual occurs in response to repeated exposure to a visual cue.

No homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
No homologous proteins
10 20 30 40 50 60
MDPKDRKKIQ FSVPAPPSQL DPRQVEMIRR RRPTPAMLFR LSEHSSPEEE ASPHQRASGE
70 80 90 100 110 120
GHHLKSKRPN PCAYTPPSLK AVQRIAESHL QSISNLNENQ ASEEEDELGE LRELGYPREE
130 140 150 160 170 180
DEEEEEDDEE EEEEEDSQAE VLKVIRQSAG QKTTCGQGLE GPWERPPPLD ESERDGGSED
190 200
QVEDPALSEP GEEPQRPSPS EPGT