MYH8

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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
Gene location (Human)
Chromosome 17 (human)
Chr.Chromosome 17 (human)[1]
Chromosome 17 (human)
Genomic location for MYH8
Genomic location for MYH8
Band17p13.1Start10,390,322 bp[1]
End10,421,950 bp[1]
RNA expression pattern
PBB GE MYH8 34471 at fs.png

PBB GE MYH8 206717 at fs.png
More reference expression data
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: 67.28 – 67.31 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[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000133020 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000055775 - Ensembl, 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[edit]