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10998 SLC27A5

10998

SLC27A5

solute carrier family 27 member 5

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 27 member 5

研究结论

Date Results Publications
2013-06-15 12:06:00 Based on a study of 10 pediatric patients, genetic defects that disrupt bile acid amidation cause fat-soluble vitamin deficiency and growth failure, indicating the importance of bile acid conjugation in lipid absorption. 23415802
2012-08-11 11:28:00 Bile acid-CoA ligase deficiency is a new inborn error of bile acid metabolism [case report] 22089923
2011-03-05 10:42:00 A promoter polymorphism in the FATP5 is associated with the metabolic syndrome and steatosis. 20945272
2010-12-05 22:08:00 Observational study of gene-disease association. (HuGE Navigator) 20945272
2008-03-13 09:02:00 Observational study of gene-disease association. (HuGE Navigator) 17266179

名称对应

Type IDs
Synonymous ACSB, ACSVL6, BACS, BAL, FACVL3, FATP-5, FATP5, VLACSR, VLCS-H2, VLCSH2
Gene
UniProtKB-ID: S27A5_HUMAN
UniprotKB: Q9Y2P5
UniParc: UPI0000072ECE, UPI00017A76E4
EMBL: AK298446, AK123036, AF064255, AC012313, CH471135
Ensembl: ENSG00000083807
KO: hsa:10998
Nucleutide sequences
EMBL-CDS: EAW72601.1, BAG53858.1, BAG60663.1, AAD29444.1
Ensembl_TRS: ENST00000263093, ENST00000601355
Protein sequencees
Ensembl_PRO: ENSP00000263093, ENSP00000470368
RefSeq: NP_001308125.1, NP_036386.1, XP_011524666.1, XP_016881703.1
Others
UniRef100: UniRef100_Q9Y2P5
UniRef90: UniRef90_Q9Y2P5
UniRef50: UniRef50_Q9Y2P5
UniGene: Hs.292177
CCDS: CCDS12983.1, CCDS82415.1

全选

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研究热度

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