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MYH8

From Wikipedia, the free encyclopedia
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
View/Edit HumanView/Edit Mouse

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

Mutations in MYH8 are associated with Trismus pseudocamptodactyly syndrome.


References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000133020Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000055775Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Karsch-Mizrachi I, Feghali R, Shows TB, Leinwand LA (Aug 1990). "Generation of a full-length human perinatal myosin heavy-chain-encoding cDNA". Gene. 89 (2): 289–94. doi:10.1016/0378-1119(90)90020-R. PMID 2373371.
  6. ^ "Entrez Gene: MYH8 myosin, heavy chain 8, skeletal muscle, perinatal".

Further reading

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