Type | Description |
---|---|
Definition | G protein regulated inducer of neurite outgrowth 2 |
Date | Results | Publications |
---|---|---|
2019-01-19 11:48:00 | Four of these 16 variants were rare damaging mutations including novel mutations in KCNJ12/KCNJ18, and GPRIN2 genes. This WES study in Iranian patients with ESCC, provides insight into the identification of novel germline mutations in familial ESCC. Our data suggest an association between specific mutations and increased risk of ESCC | 29405996 |
Type | IDs |
---|---|
Synonymous | GRIN2, KIAA0514 |
Gene |
UniProtKB-ID:
GRIN2_HUMAN
UniprotKB:
O60269
UniParc:
UPI000013ECB4
EMBL:
AL645529,
AB011086,
BC011672
Ensembl:
ENSG00000204175
KO:
hsa:9721
|
Nucleutide sequences |
EMBL-CDS:
AAH11672.1,
BAA25440.2
Ensembl_TRS:
ENST00000374314,
ENST00000374317
|
Protein sequencees |
Ensembl_PRO:
ENSP00000363436,
ENSP00000363433
RefSeq:
NP_001372216.1,
XP_011538690.1,
NP_001372211.1,
NP_001372225.1,
NP_001372207.1,
NP_001372229.1,
NP_001372223.1,
NP_001372205.1,
NP_001372226.1,
XP_016872465.1,
NP_001372209.1,
NP_001372212.1,
XP_016872467.1,
XP_016872464.1,
XP_016872468.1,
NP_001372228.1,
NP_001372208.1,
NP_001372206.1,
NP_055511.2,
XP_016872463.1,
NP_001372218.1,
XP_016872470.1,
NP_001372224.1,
NP_001372222.1,
XP_016872466.1,
NP_001372227.1,
XP_016872469.1,
XP_016872472.1,
NP_001372220.1,
XP_016872471.1,
NP_001372230.1,
NP_001372210.1,
NP_001372204.1,
XP_016872473.1
|
Others |
UniRef100:
UniRef100_O60269
UniRef90:
UniRef90_O60269
UniRef50:
UniRef50_O60269
UniGene:
Hs.523375
CCDS:
CCDS73101.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
---|---|---|---|---|---|---|---|---|
Refseq |
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