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3788 KCNS2

3788

KCNS2

potassium voltage-gated channel modifier subfamily S member 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition potassium voltage-gated channel modifier subfamily S member 2

研究结论

Date Results Publications
2019-10-26 10:48:00 KCNS2 mutation is associated with Essential Tremor. 29769701

名称对应

Type IDs
Synonymous KV9.2
Gene
UniProtKB-ID: KCNS2_HUMAN
UniprotKB: Q9ULS6
UniParc: UPI0000001653
EMBL: BC034778, BC027932, AK293096, AB032970, CH471060
Ensembl: ENSG00000156486
KO: hsa:3788
Nucleutide sequences
EMBL-CDS: BAA86458.1, EAW91780.1, AAH27932.1, AAH34778.1, BAF85785.1
Ensembl_TRS: ENST00000287042, ENST00000521839
Protein sequencees
Ensembl_PRO: ENSP00000430712, ENSP00000287042
RefSeq: NP_065748.1
Others
UniRef100: UniRef100_Q9ULS6
UniRef90: UniRef90_Q9ULS6
UniRef50: UniRef50_O35174
UniGene: Hs.388045
CCDS: CCDS6279.1

全选

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