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79734 KCTD17

79734

KCTD17

potassium channel tetramerization domain containing 17

protein-coding

Homo sapiens

基因描述

Type Description
Definition potassium channel tetramerization domain containing 17

研究结论

Date Results Publications
2015-08-22 10:49:00 A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia. 25983243

名称对应

Type IDs
Gene
UniProtKB-ID: KCD17_HUMAN, A0A087WX35_HUMAN
UniprotKB: Q8N5Z5, A0A087WX35
UniParc: UPI0001EED0F3, UPI0001610FBA, UPI0000EE5BFA
EMBL: BC025403, CH471095, BC031038, AL022314, KF457441, AK022304
Ensembl: ENSG00000100379
KO: hsa:79734
Nucleutide sequences
EMBL-CDS: AAH25403.1, BAB14007.1, AAH31038.1, EAW60139.1
Ensembl_TRS: ENST00000403888, ENST00000402077, ENST00000610767
Protein sequencees
Ensembl_PRO: ENSP00000385096, ENSP00000384391, ENSP00000480699
RefSeq: NP_078957.2, NP_001269614.1, XP_005261799.2, XP_005261798.2, XP_005261801.1, NP_001269613.1, XP_005261800.2, XP_011528676.1, XP_011528679.1, NP_001269615.1
Others
UniRef100: UniRef100_A0A087WX35, UniRef100_Q8N5Z5
UniRef90: UniRef90_Q8N5Z5, UniRef90_A0A337SQW8
UniRef50: UniRef50_A0A2K5HQ31, UniRef50_Q8N5Z5
UniGene: Hs.517597
CCDS: CCDS74854.1, CCDS13940.2

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