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2618 GART

2618

GART

phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase

protein-coding

Homo sapiens

基因描述

Type Description
Definition phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase

研究结论

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

名称对应

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

全选

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