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212919 Kctd7

212919

Kctd7

potassium channel tetramerisation domain containing 7

protein-coding

Mus musculus

基因描述

Type Description
Definition potassium channel tetramerisation domain containing 7

研究结论

Date Results Publications
2020-05-16 10:04:00 Deletion of Kctd7 induces defective patterning of the adult mouse retina vascular network, resulting in increased branching, vessel length, and lacunarity. These alterations reflect early and specific defects in vessel development, as emergence of the superficial and deep vascular layers were delayed. These defects are likely due to a role for Kctd7 in inner retina neurons. 31175897
2011-11-05 12:51:00 KCTD7 expression hyperpolarizes the cell membrane and reduces the excitability of transfected neurons in patch clamp experiments. 21710140

名称对应

Type IDs
Synonymous 4932409E18, 9430010P06Rik
Gene
UniProtKB-ID: KCTD7_MOUSE
UniprotKB: Q8BJK1
UniParc: UPI0000024EED
EMBL: AK083583, AK140606, BC051544, CH466529, BC141201, BC139070, AK029942
Ensembl: ENSMUSG00000034110
KO: mmu:212919
Nucleutide sequences
EMBL-CDS: AAH51544.1, AAI41202.1, BAC38959.1, AAI39071.1, BAC26691.1, EDL19476.1, BAE24427.1
Ensembl_TRS: ENSMUST00000040616
Protein sequencees
Ensembl_PRO: ENSMUSP00000044568
RefSeq: XP_036020874.1, XP_006504464.1, NP_766097.1
Others
UniRef100: UniRef100_Q8BJK1
UniRef90: UniRef90_Q8BJK1
UniRef50: UniRef50_Q96MP8
UniGene: Mm.55812
CCDS: CCDS19707.1

全选

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研究热度

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