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4625 MYH7

4625

MYH7

myosin heavy chain 7

protein-coding

Homo sapiens

基因描述

Type Description
Definition myosin heavy chain 7

研究结论

Date Results Publications
2021-01-23 12:58:00 Generation of a hiPSC line ZZUNEUi007-A from a patient with hypertrophic cardiomyopathy caused by mutation in MYH7. 31931472
2021-01-09 13:31:00 Genetic screening for hypertrophic cardiomyopathy in large, asymptomatic military cohorts. 32030882
2021-01-09 13:27:00 Mutation-specific pathology and treatment of hypertrophic cardiomyopathy in patients, mouse models and human engineered heart tissue. 32217077
2020-12-12 13:23:00 A new mutation affecting the converter region of the beta-myosin heavy chain related to hypertrophic cardiomyopathy with poor prognosis. 31416728
2020-11-21 13:20:00 Hypertrophic cardiomyopathy MYH7 mutation R723G alters mRNA secondary structure. 31790337

名称对应

Type IDs
Synonymous CMD1S, CMH1, MPD1, MYHCB, SPMD, SPMM
Gene
UniProtKB-ID: MYH7_HUMAN
UniprotKB: P12883
UniParc: UPI000014019B
EMBL: X04632, BC112173, X51591, X04628, M17712, X52889, M21665, X04629, M58018, X04630, X04631, M25135, EU747717, EF179180, X05631, X04627, BC112171, M27636, X03741, X06976, M25133, AJ238393, CH471078, M25134, M57965, X04633
Ensembl: ENSG00000092054
KO: hsa:4625
Nucleutide sequences
EMBL-CDS: CAA27381.1, CAA29119.1, AAI12174.1, CAC20413.1, AAA36343.1, AAA79019.1, ACH92815.1, AAI12172.1, EAW66152.1, CAA30039.1, AAA60384.1, AAA51837.1, AAA36345.1, CAA35940.1, AAA62830.1, CAA28300.1, ABN05283.1, CAA37068.1
Ensembl_TRS: ENST00000355349
Protein sequencees
Ensembl_PRO: ENSP00000347507
RefSeq: NP_000248.2, XP_016876829.1
Others
UniRef100: UniRef100_P12883
UniRef90: UniRef90_P12883
UniRef50: UniRef50_P12883
UniGene: Hs.719946
CCDS: CCDS9601.1

全选

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