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4648 MYO7B

4648

MYO7B

myosin VIIB

protein-coding

Homo sapiens

基因描述

Type Description
Definition myosin VIIB

研究结论

Date Results Publications
2018-04-28 11:54:00 The structure of the Myo7b CMF/USH1C PDZ complex provides mechanistic explanations for >20 deafness-causing mutations in Myo7a CMF. Taken together, these findings suggest that binding to PDZ domains, such as those from USH1C, PDZD7, and Whirlin, is a common property of CMFs of Myo7a, Myo7b, and Myo15a. 28439001
2010-04-07 21:39:00 Observational study of gene-disease association. (HuGE Navigator) 20198315
2010-04-07 21:39:00 Observational study of gene-disease association. (HuGE Navigator) 19724895
2010-04-07 21:39:00 Observational study of gene-disease association. (HuGE Navigator) 20237496
2010-01-21 00:00:00 Data revealed that six polymorphisms of F10, PITRM1, PCSK2, JPH3, MYO7B, and AKAP12 were related (P<0.05) to the prevalence of chronic kidney disease. 19724895

名称对应

Type IDs
Gene
UniProtKB-ID: MYO7B_HUMAN
UniprotKB: Q6PIF6
UniParc: UPI000170BA4C, UPI00006C04F0
EMBL: AK074183, AC010976, BC035615, L29147
Ensembl: ENSG00000169994
KO: hsa:4648
Nucleutide sequences
EMBL-CDS: BAB85009.1, AAH35615.2, AAA20910.1
Ensembl_TRS: ENST00000428314, ENST00000409816
Protein sequencees
Ensembl_PRO: ENSP00000386461, ENSP00000415090
RefSeq: XP_016859658.1, XP_006712602.1, NP_001073996.1, XP_011509520.1
Others
UniRef100: UniRef100_Q6PIF6
UniRef90: UniRef90_Q6PIF6
UniRef50: UniRef50_Q6PIF6
UniGene: Hs.154578, Hs.677195
CCDS: CCDS46405.1

全选

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研究热度

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