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387601 SLC22A25

387601

SLC22A25

solute carrier family 22 member 25

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 22 member 25

研究结论

Date Results Publications
2018-07-28 10:45:00 TNFSF13, SLC22A25 and SALL4 may thus be novel susceptibility loci for atrial fibrillation in the Japanese population 28849223
2010-01-21 00:00:00 Review summarizes current knowledge on the functional and phenotypic consequences of genetic variation in intestinally, hepatically and renally expressed members of solute carrier family (SLC) member 25. 18466105
2010-01-21 00:00:00 cloning of a novel human slc22 family member, UST6, expressed exclusively in liver in both embryo and adult, is reported [UST6] 15054140

名称对应

Type IDs
Synonymous HIMTP, UST6
Gene
UniProtKB-ID: S22AP_HUMAN
UniprotKB: Q6T423
UniParc: UPI00001A72A5
EMBL: AP003420, BC101316, AP001880, AY437532
Ensembl: ENSG00000196600
KO: hsa:387601
Nucleutide sequences
EMBL-CDS: AAI01317.1, AAR84082.1
Ensembl_TRS: ENST00000306494
Protein sequencees
Ensembl_PRO: ENSP00000307443
RefSeq: NP_955384.3, XP_016873175.1, XP_016873183.1, XP_016873180.1, XP_016873185.1, XP_016873178.1, XP_016873176.1, XP_016873182.1, XP_016873173.1, XP_016873181.1, XP_016873184.1, XP_016873179.1, XP_016873174.1, XP_016873177.1
Others
UniRef100: UniRef100_Q6T423
UniRef90: UniRef90_Q6T423
UniRef50: UniRef50_Q8IVM8
UniGene: Hs.332119
CCDS: CCDS31592.1

全选

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研究热度

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