MYH8

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Myosin-8 is a protein that in humans is encoded by the MYH8 gene.[5][6]

AliasesMYH8, MyHC-peri, MyHC-pn, gtMHC-F, DA7, myosin, heavy chain 8, skeletal muscle, perinatal, myosin heavy chain 8
End10,421,950 bp[1]
Quick facts Identifiers, Aliases ...
MYH8
Identifiers
AliasesMYH8, MyHC-peri, MyHC-pn, gtMHC-F, DA7, myosin, heavy chain 8, skeletal muscle, perinatal, myosin heavy chain 8
External IDsOMIM: 160741; MGI: 1339712; HomoloGene: 68256; GeneCards: MYH8; OMA:MYH8 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002472

NM_177369

RefSeq (protein)

NP_002463

NP_796343

Location (UCSC)Chr 17: 10.39 – 10.42 MbChr 11: 67.17 – 67.2 Mb
PubMed search[3][4]
Wikidata
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Mutations in MYH8 are associated with Trismus pseudocamptodactyly syndrome.


References

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