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240595 Kcnv2

240595

Kcnv2

potassium channel, subfamily V, member 2

protein-coding

Mus musculus

基因描述

Type Description
Definition potassium channel, subfamily V, member 2

研究结论

Date Results Publications
2019-05-25 11:00:00 Kv8.2 knock-out (KO) mice show many similarities to human cone dystrophy with a supernormal rod response, including a depressed a-wave and an elevated b-wave response with bright light stimulation. Optical coherence tomography imaging and immunohistochemistry indicate that the changes in six-month-old Kv8.2 KO retinae are largely limited to the outer nuclear layer, while outer segments appear intact. 30820446
2014-07-26 12:44:00 We conclude that nucleotide changes in evolutionary conserved crx binding site could impact retina-specific expression levels of Kcnv2. 24664678
2013-03-02 13:12:00 two pore mutations (W467G and G478R) led to the formation of nonconducting heteromeric Kv2.1/Kv8.2 channels 23115240
2011-06-18 11:33:00 Results demonstrate that altered potassium subunit function influences epilepsy susceptibility and implicate Kcnv2 as an epilepsy gene. 21402906
2010-01-21 00:00:00 Kcnv2 is a strong functional candidate for epilepsy modifier. 19513789

名称对应

Type IDs
Synonymous KV11.1
Gene
UniProtKB-ID: KCNV2_MOUSE
UniprotKB: Q8CFS6
UniParc: UPI00000E8F84
EMBL: BC039042, AY238939
Ensembl: ENSMUSG00000047298
KO: mmu:240595
Nucleutide sequences
EMBL-CDS: AAH39042.1, AAP70480.1
Ensembl_TRS: ENSMUST00000056708
Protein sequencees
Ensembl_PRO: ENSMUSP00000055091
RefSeq: NP_899002.1, XP_006527130.1
Others
UniRef100: UniRef100_Q8CFS6
UniRef90: UniRef90_Q8CFS6
UniRef50: UniRef50_Q8TDN2
UniGene: Mm.269759
CCDS: CCDS29722.1

全选

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研究热度

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