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4626 MYH8

4626

MYH8

myosin heavy chain 8

protein-coding

Homo sapiens

基因描述

Type Description
Definition myosin heavy chain 8

研究结论

Date Results Publications
2021-04-03 13:31:00 Novel MYH8 mutations in 152 Han Chinese samples with ovarian endometriosis. 32308057
2021-03-13 13:26:00 Novel exomic rare variants associated with venous thrombosis. 32232851
2020-10-31 13:12:00 Truncation of MYH8 tail in AML: a novel prognostic marker with increase cell migration and epithelial-mesenchymal transition utilizing RAF/MAPK pathway. 31430364
2018-05-05 10:08:00 There was an immediate shutdown of the MHC IIX gene after resistance exercise. Silencing of the MHC IIX gene is sustained at least 4 days after removal of the stimulus. 28508505
2017-08-12 10:31:00 Loss-of-function variants in the MYH8 gene do not cause autosomal dominant trismus-pseudocamptodactyly syndrome. 28377322

名称对应

Type IDs
Synonymous DA7, MyHC-peri, MyHC-pn, gtMHC-F
Gene
UniProtKB-ID: MYH8_HUMAN
UniprotKB: P13535
UniParc: UPI000012FB7D
EMBL: Z38133, AF067143, X51592, M36769
Ensembl: ENSG00000133020
KO: hsa:4626
Nucleutide sequences
EMBL-CDS: AAC17185.1, CAA35941.1, AAC21557.1, CAA86293.1
Ensembl_TRS: ENST00000403437
Protein sequencees
Ensembl_PRO: ENSP00000384330
RefSeq: NP_002463.2
Others
UniRef100: UniRef100_P13535
UniRef90: UniRef90_P13535
UniRef50: UniRef50_P13535
UniGene: Hs.700484
CCDS: CCDS11153.1

全选

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研究热度

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