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63027 SLC22A23

63027

SLC22A23

solute carrier family 22 member 23

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 22 member 23

研究结论

Date Results Publications
2015-05-09 11:03:00 Genetic variations in the SLC22A23 locus contribute to the susceptibility to inflammatory bowel disease in a small fraction of white patients. 24740203
2010-12-05 22:08:00 Observational study of gene-disease association. (HuGE Navigator) 19760754
2010-12-05 22:08:00 Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) 20886065
2010-12-05 22:08:00 Observational study of gene-disease association. (HuGE Navigator) 21072187
2010-12-05 22:08:00 Observational study and genome-wide association study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) 20921969

名称对应

Type IDs
Synonymous C6orf85
Gene
UniProtKB-ID: S22AN_HUMAN, Q9UFY2_HUMAN
UniprotKB: A1A5C7, Q9UFY2
UniParc: UPI0000EE5391, UPI0000EA3419, UPI000007373E, UPI00015D773E, UPI000004B693
EMBL: AL445309, AL110245, BC040876, AL160398, BC128580, AK172770, BC128581
Ensembl: ENSG00000137266
KO: hsa:63027
Nucleutide sequences
EMBL-CDS: AAI28582.1, AAH40876.1, AAI28581.1, BAD18753.1, CAB53695.1
Ensembl_TRS: ENST00000490273, ENST00000406686, ENST00000380298, ENST00000380302
Protein sequencees
Ensembl_PRO: ENSP00000369657, ENSP00000419463, ENSP00000369653, ENSP00000385028
RefSeq: NP_056297.1, NP_001369247.1, XP_016866675.1, NP_001273384.1, XP_016866672.1, XP_016866674.1, NP_001273385.1, XP_011513103.1, NP_001369246.1, XP_016866669.1, NP_001369250.1, NP_001369249.1, NP_001369248.1, NP_068764.3, XP_016866673.1, XP_016866670.1
Others
UniRef100: UniRef100_Q9UFY2, UniRef100_A1A5C7
UniRef90: UniRef90_A1A5C7, UniRef90_Q9UFY2
UniRef50: UniRef50_Q9UFY2, UniRef50_A1A5C7
UniGene: Hs.713588
CCDS: CCDS75389.1, CCDS47363.1, CCDS34331.1

全选

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