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4632 MYL1

4632

MYL1

myosin light chain 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition myosin light chain 1

研究结论

Date Results Publications
2019-05-11 13:30:00 Our data implicate MYL1 as a crucial protein for adequate skeletal muscle function and that MYL1 deficiency is associated with severe congenital myopathy. 30215711
2018-04-07 11:55:00 MLCK and phosphorylated MLC are potential prognostic indicators of leiomyosarcoma. 28618653
2018-03-10 10:49:00 these results provide new insights into the sequences and modifications of myosin light chain isoforms in the human and swine hearts, which will pave the way for a better understanding of their functional roles in cardiac physiology and pathophysiology. 28427997
2018-01-06 11:05:00 These results support the concept of the ATP-induced transient interaction of the essential light chain-1 N-terminus with the motor domain of the myosin head. 29102634
2017-04-15 10:09:00 polymorphism of intron MYL1 was associated with endurance performance, specifically in endurance trainability, but not genetic predisposition, in human adults. 26473445

名称对应

Type IDs
Synonymous MLC1F, MLC3F
Gene
UniProtKB-ID: MYL1_HUMAN
UniprotKB: P05976
UniParc: UPI0000000C6C, UPI000013E94F
EMBL: CH471063, M20643, BC005318, AK311892, X05451, AK311942, X05450, J05026, CR456869, M20642
Ensembl: ENSG00000168530
KO: hsa:4632
Nucleutide sequences
EMBL-CDS: EAW70483.1, EAW70484.1, CAA29020.1, AAA66960.1, CAG33150.1, AAA59854.1, AAH05318.1, AAA59855.1, BAG34833.1, BAG34883.1, CAB42646.1
Ensembl_TRS: ENST00000341685, ENST00000352451
Protein sequencees
Ensembl_PRO: ENSP00000343321, ENSP00000307280
RefSeq: NP_524144.1, NP_524146.1
Others
UniRef100: UniRef100_P05976
UniRef90: UniRef90_P05976
UniRef50: UniRef50_P05976
UniGene: Hs.187338
CCDS: CCDS2391.1, CCDS2390.1

全选

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研究热度

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