Type | Description |
---|---|
Definition | glutamate decarboxylase 1 |
Date | Results | Publications |
---|---|---|
2021-01-02 12:52:00 | Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants. | 32705143 |
2020-12-19 13:40:00 | Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy. | 32282878 |
2020-11-28 13:14:00 | GAD1 but not GAD2 polymorphisms are associated with heroin addiction phenotypes. | 31866536 |
2020-08-12 14:40:00 | The methylation level near the CTCF-binding site of GAD1 and GAD1 mRNA expression level were significantly higher in lung adenocarcinoma (LADC) tumors than in paired non-tumorous tissues. Patients with GAD1-overexpressing LADC showed poorer prognosis suggesting that it might be useful biomarker to stratify patients with worse clinical outcomes after resection. | 31207151 |
2020-03-14 11:11:00 | GAD1 allelic variation moderated early sensory processes (N2a) in the subsample and influenced late cognitive processes (P3b). | 30488987 |
Type | IDs |
---|---|
Synonymous | CPSQ1, GAD, SCP |
Gene |
UniProtKB-ID:
DCE1_HUMAN,
Q8IVA8_HUMAN,
A0A0S2Z3V5_HUMAN
UniprotKB:
Q99259,
Q8IVA8,
A0A0S2Z3V5
UniParc:
UPI000007466A,
UPI000056F173,
UPI000002D729,
UPI0000072E8D
EMBL:
M81883,
AY337516,
M55574,
S61897,
M70434,
BC036552,
M86522,
BC026349,
L16888,
AF178853,
BC037780,
AC007405,
KU178086,
BC002815,
S61898,
CH471058,
Z22750
Ensembl:
ENSG00000128683
KO:
hsa:2571
|
Nucleutide sequences |
EMBL-CDS:
AAA52512.1,
AAA35900.1,
AAH02815.1,
AAB26938.1,
AAB59427.1,
EAX11229.1,
AAB26937.1,
AAY24237.1,
AAF18390.2,
EAX11228.1,
AAP88035.1,
AAA62368.1,
AAH36552.1,
AAH26349.1,
AAA72938.1,
CAA80435.1,
AAH37780.1,
ALQ33544.1
Ensembl_TRS:
ENST00000625689,
ENST00000493875,
ENST00000344257,
ENST00000358196,
ENST00000375272
|
Protein sequencees |
Ensembl_PRO:
ENSP00000364421,
ENSP00000350928,
ENSP00000341167,
ENSP00000434696,
ENSP00000486612
RefSeq:
XP_016859246.1,
XP_005246501.1,
NP_038473.2,
XP_016859247.1,
XP_024308551.1,
XP_016859245.1,
NP_000808.2,
XP_011509224.1
|
Others |
UniRef100:
UniRef100_Q8IVA8,
UniRef100_Q99259
UniRef90:
UniRef90_Q99259
UniRef50:
UniRef50_Q05329
UniGene:
Hs.420036
CCDS:
CCDS2239.1,
CCDS2240.1
|
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