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106931 Kctd1

106931

Kctd1

potassium channel tetramerisation domain containing 1

protein-coding

Mus musculus

基因描述

Type Description
Definition potassium channel tetramerisation domain containing 1

研究结论

Date Results Publications
2020-02-29 10:39:00 KCTD1 promotes adipogenesis through the interaction with transcription factor AP2 alpha and by removing it from the nucleus. 31465887
2018-06-23 10:26:00 The main pathological phenotype of the Kctd1 (I27N) heterozygous mutant mice consists of kidney dysfunction and secondary effects thereof, without gross additional primary alterations in the other phenotypic parameters analyzed. 28818080

名称对应

Type IDs
Synonymous 4933402K10Rik, AI661543, AW553000
Gene
UniProtKB-ID: KCTD1_MOUSE, E9Q6T9_MOUSE
UniprotKB: Q5M956, E9Q6T9
UniParc: UPI00001CDFF1, UPI00004CEEEF, UPI0000607DC3
EMBL: AY899808, AC102342, AC125091, AC102409, BC087623
Ensembl: ENSMUSG00000036225
KO: mmu:106931
Nucleutide sequences
EMBL-CDS: AAW88504.1, AAH87623.1
Ensembl_TRS: ENSMUST00000025992, ENSMUST00000168989
Protein sequencees
Ensembl_PRO: ENSMUSP00000025992, ENSMUSP00000128070
RefSeq: NP_598873.2, XP_036016811.1, XP_006525548.1, NP_001136203.1
Others
UniRef100: UniRef100_Q719H9, UniRef100_E9Q6T9
UniRef90: UniRef90_Q719H9, UniRef90_Q8R4G8
UniRef50: UniRef50_Q719H9, UniRef50_Q8R4G8
UniGene: Mm.329299
CCDS: CCDS50229.1

全选

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研究热度

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