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22989 MYH15

22989

MYH15

myosin heavy chain 15

protein-coding

Homo sapiens

基因描述

Type Description
Definition myosin heavy chain 15

研究结论

Date Results Publications
2020-03-14 10:46:00 Rare variants in MYH15 represent a likely genetic risk factor for amyotrophic lateral sclerosis. Furthermore, MYH15 could modulate the toxicity of dipeptides produced from expanded G4C2 repeat. 30985904
2019-07-27 11:27:00 This is the first study to report the association of MYH15 gene polymorphisms with asthma. Polymorphisms of rs9288876, rs7635009, and rs1454197 altered transcriptional regulation of MYH15 and may be functional variants conferring susceptibility to asthma 30906771
2017-03-22 10:19:00 MYH15 expression is significantly downregulated in human masticatory mucosa during wound healing 28005267
2012-04-26 16:08:00 A protein encoded by this locus was found to be differentially expressed in postmortem brains from patients with atypical frontotemporal lobar degeneration. 22360420
2010-04-07 21:39:00 Observational study of gene-disease association. (HuGE Navigator) 19752551

名称对应

Type IDs
Gene
UniProtKB-ID: MYH15_HUMAN
UniprotKB: Q9Y2K3
UniParc: UPI0000253B6F
EMBL: AB023217, AC069499
Ensembl: ENSG00000144821
KO: hsa:22989
Nucleutide sequences
EMBL-CDS: BAA76844.3
Ensembl_TRS: ENST00000273353
Protein sequencees
Ensembl_PRO: ENSP00000273353
RefSeq: NP_055796.1, XP_016861411.1, XP_011510861.1
Others
UniRef100: UniRef100_Q9Y2K3
UniRef90: UniRef90_Q9Y2K3
UniRef50: UniRef50_Q9Y2K3
UniGene: Hs.731060
CCDS: CCDS43127.1

全选

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研究热度

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