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56996 SLC12A9

56996

SLC12A9

solute carrier family 12 member 9

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 12 member 9

研究结论

Date Results Publications
2013-06-15 10:58:00 Review summarizes three human disorders that have been linked to the mutation/dysfunction of Na-Cl, Na-K-2Cl, and K-Cl cotransporters (Bartter's, Gitleman's, and Andermann's syndromes). 23325410
2010-09-15 22:06:00 Observational study, meta-analysis, and genome-wide association study of gene-disease association. (HuGE Navigator) 20639392

名称对应

Type IDs
Synonymous CCC6, CIP1, WO3.3, hCCC6
Gene
UniProtKB-ID: S12A9_HUMAN, Q9H7I6_HUMAN
UniprotKB: Q9BXP2, Q9H7I6
UniParc: UPI0002064E33, UPI000006E663, UPI00000708D7, UPI000006CD28, UPI000006E2CD
EMBL: AB033284, AK301411, BC000154, AF284422, CH236956, AC011895, AF312032, AK024494, CH471091
Ensembl: ENSG00000146828
KO: hsa:56996
Nucleutide sequences
EMBL-CDS: AAK21009.1, AAF88060.1, EAW76484.1, EAW76483.1, EAW76475.1, EAW76476.1, EAW76485.1, EAW76480.1, BAB40456.1, BAH13476.1, AAH00154.1, EAL23818.1, AAK21008.1, BAB15784.1
Ensembl_TRS: ENST00000540482, ENST00000415287, ENST00000354161
Protein sequencees
Ensembl_PRO: ENSP00000443702, ENSP00000413796, ENSP00000275730
RefSeq: XP_005250559.1, XP_011514716.1, XP_006716117.1, XP_006716118.1, NP_001254741.1, NP_001254743.1, XP_005250561.1, NP_001350422.1, NP_001350423.1, NP_064631.2
Others
UniRef100: UniRef100_Q9H7I6, UniRef100_Q9BXP2
UniRef90: UniRef90_Q9BXP2, UniRef90_Q9H7I6
UniRef50: UniRef50_Q9BXP2, UniRef50_Q9BXP2-4
UniGene: Hs.521087
CCDS: CCDS59069.1, CCDS5707.1, CCDS59068.1

全选

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