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 A6NC05

Entry ID Method Resolution Chain Position Source
AF-A6NC05-F1 Predicted AlphaFoldDB

103 variants for A6NC05

Variant ID(s) Position Change Description Diseaes Association Provenance
rs1037167919
CA360820348
3 W>* No ClinGen
TOPMed
gnomAD
CA127423996
rs1037167919
CA360820347
3 W>C No ClinGen
TOPMed
gnomAD
CA127423994
rs928909666
6 G>E No ClinGen
TOPMed
gnomAD
CA127423992
rs188886844
7 N>S No ClinGen
1000Genomes
TOPMed
gnomAD
CA127423991
rs949101591
8 S>N No ClinGen
TOPMed
gnomAD
rs1212534742
CA360820308
9 M>T No ClinGen
gnomAD
rs916229349
CA127423989
9 M>V No ClinGen
TOPMed
gnomAD
rs904773366
CA127423987
11 L>I No ClinGen
gnomAD
rs529537151
CA3391132
11 L>P No ClinGen
1000Genomes
ExAC
gnomAD
rs563543864
CA3391131
13 R>G No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA360820277
rs1342155287
14 S>F No ClinGen
gnomAD
CA360820279
rs990994638
14 S>P No ClinGen
TOPMed
CA127423984
rs990994638
14 S>T No ClinGen
TOPMed
CA127423982
rs957754505
17 G>V No ClinGen
TOPMed
rs1561490318
CA360820255
18 L>F No ClinGen
Ensembl
CA360820252
rs1271822091
18 L>H No ClinGen
TOPMed
gnomAD
rs1271822091
CA360820250
18 L>R No ClinGen
TOPMed
gnomAD
CA127423980
rs912034273
24 S>C No ClinGen
TOPMed
gnomAD
rs752538265
CA127423977
26 S>F Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
Ensembl
NCI-TCGA
rs1294542197
CA360820185
28 T>A No ClinGen
gnomAD
rs1443285258
CA360820179
29 T>A No ClinGen
TOPMed
gnomAD
rs1334740160
CA360820176
29 T>N No ClinGen
gnomAD
CA360820165
rs1411438570
31 P>L No ClinGen
gnomAD
rs1329314230
CA360820168
31 P>S No ClinGen
gnomAD
TCGA novel 32 V>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA360820133
rs1295619638
36 F>S No ClinGen
TOPMed
rs1407581039
CA360820101
39 D>G No ClinGen
gnomAD
rs1159344003
CA360820095
40 P>S No ClinGen
gnomAD
rs1159344003
CA360820097
40 P>T No ClinGen
gnomAD
rs745777421
CA127422752
42 P>H No ClinGen
TOPMed
gnomAD
rs745777421
CA127422751
42 P>L No ClinGen
TOPMed
gnomAD
CA360820080
rs745777421
42 P>R No ClinGen
TOPMed
gnomAD
CA360820063
rs1323014511
45 D>N No ClinGen
TOPMed
gnomAD
CA360820042
rs1193324708
48 K>E No ClinGen
gnomAD
CA360820020
rs1248953114
51 L>V No ClinGen
gnomAD
CA360820001
rs1190556674
54 Y>H No ClinGen
TOPMed
rs769377129
CA3391116
55 E>G No ClinGen
ExAC
TOPMed
gnomAD
CA127422743
rs777748493
56 N>D No ClinGen
TOPMed
gnomAD
rs1046482109
CA127421911
59 P>A No ClinGen
Ensembl
rs1012737090
CA360819295
59 P>H No ClinGen
TOPMed
gnomAD
CA127421909
rs1012737090
59 P>R No ClinGen
TOPMed
gnomAD
CA360819289
rs1361769345
60 Y>C No ClinGen
TOPMed
gnomAD
rs1157896711
CA360819284
61 K>E No ClinGen
gnomAD
rs1419239018
CA360819281
61 K>T No ClinGen
gnomAD
rs1049100522
CA127421908
62 D>V No ClinGen
TOPMed
CA3391088
rs780381548
63 Q>K No ClinGen
ExAC
gnomAD
rs1366013349
CA360819263
64 K>Q No ClinGen
TOPMed
CA127421904
rs994790935
65 L>Q No ClinGen
TOPMed
gnomAD
COSM4159385
rs753391035
CA127421902
66 P>A thyroid [Cosmic] No ClinGen
cosmic curated
TOPMed
gnomAD
rs897944746
CA360819237
68 T>K No ClinGen
TOPMed
gnomAD
CA127421900
rs897944746
68 T>R No ClinGen
TOPMed
gnomAD
rs1210583797
CA360819218
71 R>K No ClinGen
TOPMed
gnomAD
rs534484470
CA3391087
72 R>C No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA3391086
rs750575443
72 R>H No ClinGen
ExAC
gnomAD
CA360819205
rs1385104006
73 S>F No ClinGen
TOPMed
CA360819208
rs1238610823
73 S>T No ClinGen
TOPMed
gnomAD
rs1299146562
CA360819193
75 S>F No ClinGen
TOPMed
CA127421893
rs575131354
76 S>* No ClinGen
1000Genomes
TOPMed
CA360819182
rs1232521760
77 P>L No ClinGen
TOPMed
gnomAD
CA360819171
rs1297271034
79 H>R No ClinGen
gnomAD
CA360819164
rs1324774663
80 P>L No ClinGen
TOPMed
gnomAD
TCGA novel 80 P>S Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1042580301
CA127421889
81 H>D No ClinGen
gnomAD
rs1042580301
CA360819161
81 H>N No ClinGen
gnomAD
rs1490051471
CA360819149
82 M>I No ClinGen
TOPMed
rs369567694
CA3391084
82 M>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1207518613
CA360819141
83 A>V No ClinGen
TOPMed
CA127421885
rs987279680
85 Q>P No ClinGen
Ensembl
CA3391082
rs537960991
86 S>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1426598712
CA360819109
88 K>N No ClinGen
gnomAD
rs539226324
CA127421881
91 N>S No ClinGen
Ensembl
rs1204581719
CA360819085
92 L>V No ClinGen
gnomAD
CA360819070
rs1365147966
94 L>S No ClinGen
TOPMed
rs1561486818
CA360819057
96 Q>E No ClinGen
Ensembl
CA360819049
rs1456492968
97 V>I No ClinGen
TOPMed
CA360819034
rs1299949463
99 S>T No ClinGen
TOPMed
rs921650280
CA127421879
102 Y>C No ClinGen
Ensembl
CA360818987
rs1288388745
105 G>R No ClinGen
gnomAD
rs1347592296
CA360818961
109 P>A No ClinGen
gnomAD
CA360818943
rs1275749686
111 T>I No ClinGen
TOPMed
gnomAD
CA360818945
rs1275749686
111 T>K No ClinGen
TOPMed
gnomAD
CA360818916
rs1325153043
115 D>E No ClinGen
gnomAD
CA3391078
rs760298235
115 D>N No ClinGen
ExAC
gnomAD
CA360818909
rs1294256181
116 C>F No ClinGen
gnomAD
rs1330517961
CA360818913
116 C>R No ClinGen
TOPMed
CA127421876
rs750387389
117 G>E No ClinGen
Ensembl
TCGA novel 119 F>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA360818885
rs1445342704
120 Y>C No ClinGen
gnomAD
CA127421872
rs963014129
120 Y>H No ClinGen
TOPMed
rs1310687506
CA360818864
123 R>T No ClinGen
gnomAD
rs541525107
CA127421871
124 M>T No ClinGen
TOPMed
gnomAD
CA360818846
rs1174070928
125 F>L No ClinGen
TOPMed
gnomAD
CA127421869
rs539050968
126 K>R No ClinGen
1000Genomes
CA360818822
rs1194336309
129 D>H No ClinGen
TOPMed
gnomAD
CA360818821
rs1194336309
129 D>Y No ClinGen
TOPMed
gnomAD
CA127421865
rs752867000
130 M>K No ClinGen
TOPMed
gnomAD
CA360818813
rs752867000
130 M>T No ClinGen
TOPMed
gnomAD
CA127421867
rs1004768464
130 M>V No ClinGen
Ensembl
CA127421863
rs1045727282
131 T>N No ClinGen
TOPMed
rs1462961203
CA360818791
133 C>Y No ClinGen
TOPMed
rs948367057
CA127421861
134 F>S No ClinGen
TOPMed
CA3391075
rs771567552
136 P>L No ClinGen
ExAC
gnomAD
rs1265687946
CA360818755
138 Q>R No ClinGen
gnomAD

No associated diseases with A6NC05

No regional properties for A6NC05

Type Name Position InterPro Accession
No domain, repeats, and functional sites for A6NC05

Functions

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

No GO annotations of cellular component

Name Definition
No GO annotations for cellular component

No GO annotations of molecular function

Name Definition
No GO annotations for molecular function

No GO annotations of biological process

Name Definition
No GO annotations for biological process

No homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
No homologous proteins
10 20 30 40 50 60
MLWFQGNSMQ LARSSFGLFL RNCSASKTTL PVLTLFTKDP CPLCDEAKEV LKPYENRQPY
70 80 90 100 110 120
KDQKLPGTRR RRSPSSPSHP HMASQSGKRY NLTLNQVLSF DYDMGLDAPK TISSDCGAFY
130
CLRMFKSPDM TCCFYPKQ