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10144 FAM13A

10144

FAM13A

family with sequence similarity 13 member A

protein-coding

Homo sapiens

基因描述

Type Description
Definition family with sequence similarity 13 member A

研究结论

Date Results Publications
2020-11-21 13:30:00 Loss of Family with Sequence Similarity 13, Member A Exacerbates Pulmonary Fibrosis Potentially by Promoting Epithelial to Mesenchymal Transition. 32029695
2020-07-18 10:25:00 GWAS-associated variants within the FAM13A locus alter adipose FAM13A expression, which in turn, regulates adipocyte differentiation and contribute to changes in body fat distribution. 32193374
2020-04-25 12:44:00 Our results suggest that FAM13A is dispensable for adipose development and insulin sensitivity. Yet the expression of FAM13A needs to be tightly controlled in adipose precursor cells for their proper survival and downstream adipogenesis. These data provide novel insights into the link between FAM13A and obesity. 30301961
2019-12-07 12:00:00 Variant genotypes of rs9224 in the FAM13A 3'UTR may modify Lung squamous carcinoma (LUSQ) susceptibility by affecting the binding of miRNA-22-5p and predict a poor prognosis of patients with LUSQ. 31539274
2019-11-16 12:58:00 Data show that FAM13A is a modifier gene of Cystic Fibrosis lung phenotype regulating RhoA activity, actin cytoskeleton dynamics and epithelial-mesenchymal transition. 29239766

名称对应

Type IDs
Synonymous ARHGAP48, FAM13A1
Gene
UniProtKB-ID: FA13A_HUMAN
UniprotKB: O94988
UniParc: UPI0000481AF3, UPI0001D14750, UPI000004EC64, UPI000018DB8B, UPI000020B1AB
EMBL: AC021183, AB020721, AC108065, AK296932, AK091328, BN000265, AK027138, BC086875
Ensembl: ENSG00000138640
KO: hsa:10144
Nucleutide sequences
EMBL-CDS: BAG59483.1, BAC03636.1, AAH86875.1, BAA74937.3, CAE18110.1
Ensembl_TRS: ENST00000395002, ENST00000503556, ENST00000264344, ENST00000508369, ENST00000513837
Protein sequencees
Ensembl_PRO: ENSP00000421562, ENSP00000427189, ENSP00000264344, ENSP00000423252, ENSP00000378450
RefSeq: XP_016863116.1, XP_005262740.1, XP_016863119.1, XP_005262741.1, XP_011529818.1, NP_001252509.1, XP_016863121.1, XP_011529820.1, XP_006714120.1, NP_001252507.1, XP_016863122.1, XP_011529819.1, XP_005262738.1, XP_005262739.1, XP_016863113.1, NP_001015045.1, XP_016863115.1, XP_011529821.1, XP_016863117.1, XP_016863118.1, XP_016863114.1, NP_055698.2, XP_024309638.1, XP_016863120.1, NP_001252508.1, XP_016863123.1
Others
UniRef100: UniRef100_O94988
UniRef90: UniRef90_O94988
UniRef50: UniRef50_O94988
UniGene: Hs.97270, Hs.714536
CCDS: CCDS43251.1, CCDS58911.1, CCDS58912.1, CCDS58913.1, CCDS34029.1

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