Type | Description |
---|---|
Definition | phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase |
Date | Results | Publications |
---|---|---|
2018-02-03 10:10:00 | GART expression is up-regulated in patients with active colitis. | 27718035 |
2017-06-03 12:13:00 | The minor A allele of rs7279549 of GART is a functional risk factor for congenital heart disease in Shandong population. | 27659940 |
2015-06-20 10:04:00 | most significant association was detected for GART rs8971. Compared with individuals with the TT genotype, the age- and sex-adjusted odds ratio (OR) for developing HCC was 1.44 (95% confidence interval (CI): 1.03-2.02) among those with the CC genotype | 25318605 |
2014-10-25 10:13:00 | The current results showed that GART expression was associated with glioma grade and that high GART protein expression might be related to poor outcome. | 24444710 |
2014-08-23 11:19:00 | our clinical and in vitro data indicate that GART expression may be one of the causative factors for a poor prognosis in hepatocellular carcinoma. | 24830618 |
Type | IDs |
---|---|
Synonymous | AIRS, GARS, GARTF, PAIS, PGFT, PRGS |
Gene |
UniProtKB-ID:
PUR2_HUMAN,
Q59HH3_HUMAN
UniprotKB:
P22102,
Q59HH3
UniParc:
UPI00004F6A4E,
UPI0000132A2A,
UPI0000001C75
EMBL:
AK292560,
AF008653,
CH471079,
AK292897,
BC093641,
X54199,
BC101565,
M32082,
AB208785,
BC038958
Ensembl:
ENSG00000159131,
ENSG00000262473
KO:
hsa:2618
|
Nucleutide sequences |
EMBL-CDS:
EAX09828.1,
AAB70812.1,
EAX09829.1,
AAH93641.1,
AAA60077.1,
AAH38958.1,
EAX09826.1,
CAA38119.1,
AAI01566.1,
EAX09827.1,
BAF85586.1,
BAF85249.1,
BAD92022.1
Ensembl_TRS:
ENST00000381831,
ENST00000573055,
ENST00000575273,
ENST00000381839,
ENST00000381815,
ENST00000361093,
ENST00000571089
|
Protein sequencees |
Ensembl_PRO:
ENSP00000371253,
ENSP00000371236,
ENSP00000354388,
ENSP00000371261,
ENSP00000459532,
ENSP00000461700,
ENSP00000459391
RefSeq:
NP_780294.1,
NP_001129477.1,
XP_011527828.1,
NP_001129478.1,
XP_005260998.1,
XP_006724052.1,
XP_006724053.1,
NP_000810.1
|
Others |
UniRef100:
UniRef100_P22102,
UniRef100_B4DJ93
UniRef90:
UniRef90_P22102
UniRef50:
UniRef50_P22102
UniGene:
Hs.473648
CCDS:
CCDS13627.1,
CCDS13628.1
|
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Refseq |
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