Type | Description |
---|---|
Definition | T cell activation RhoGTPase activating protein |
Date | Results | Publications |
---|---|---|
2019-05-04 10:46:00 | These findings indicate that increased TAGAP expression is a distinguishing feature of inflammatory disease and further highlight the role of TAGAP in rheumatoid arthritis susceptibility. | 29017772 |
2018-02-03 11:07:00 | This is the first comprehensive study, where TAGAP gene variants were analyzed using in silico tools hence will be of great help while considering large scale studies and also in developing precision medicines for cure of diseases related to these polymorphisms | 29329296 |
2017-11-11 14:15:00 | Results suggested that TAGAP rs1738074 polymorphism could be considered as a risk factor in the prevalence of multiple sclerosis in the Iranian population | 28356229 |
2017-06-24 12:28:00 | meta-analysis provides robust estimates that polymorphisms in LPP and TAGAP genes are potential risk factors for celiac disease in Europeans and Americans | 28208589 |
2016-12-17 10:46:00 | IL2RA and TAGAP are novel vitamin D target genes. The vitamin D response is observed in samples from both the multiple sclerosis (MS) patients and controls, and is not dependent on the genotype of MS-associated SNPs in the respective genes. | 26765264 |
Type | IDs |
---|---|
Synonymous | ARHGAP47, FKSG15, IDDM21, TAGAP1 |
Gene |
UniProtKB-ID:
TAGAP_HUMAN
UniprotKB:
Q8N103
UniParc:
UPI00000708A3,
UPI000007174C,
UPI00000711C5,
UPI0000071CD5
EMBL:
AK097090,
BC111731,
AL035530,
BC015859,
AF385429,
AF314817,
AF385430
Ensembl:
ENSG00000164691
KO:
hsa:117289
|
Nucleutide sequences |
EMBL-CDS:
AAM43831.1,
AAI11732.1,
AAH15859.1,
AAL16675.1,
AAM43830.1,
BAC04947.1
Gene_ORFName:
FKSG15
Ensembl_TRS:
ENST00000338313,
ENST00000326965,
ENST00000367066
|
Protein sequencees |
Ensembl_PRO:
ENSP00000322650,
ENSP00000340217,
ENSP00000356033
RefSeq:
NP_620165.1,
NP_001265662.1,
NP_687034.1,
NP_473455.2
|
Others |
UniRef100:
UniRef100_Q8N103
UniRef90:
UniRef90_Q8N103
UniRef50:
UniRef50_Q8N103
UniGene:
Hs.529984
CCDS:
CCDS5263.1,
CCDS5261.1,
CCDS5262.1
|
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Refseq |
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