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Myosin, heavy chain 8, skeletal muscle, perinatal
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| Identifiers | ||||||||||||||
| Symbol(s) | MYH8; MyHC-peri; MyHC-pn | |||||||||||||
| External IDs | OMIM: 160741 MGI: 1339712 HomoloGene: 68256 | |||||||||||||
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| RNA expression pattern | ||||||||||||||
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| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 4626 | 17885 | ||||||||||||
| Ensembl | ENSG00000133020 | ENSMUSG00000055775 | ||||||||||||
| Uniprot | P13535 | Q1WNQ0 | ||||||||||||
| Refseq | NM_002472 (mRNA) NP_002463 (protein) |
NM_177369 (mRNA) NP_796343 (protein) |
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| Location | Chr 17: 10.23 - 10.27 Mb | Chr 11: 67.09 - 67.12 Mb | ||||||||||||
| Pubmed search | [1] | [2] | ||||||||||||
Myosin, heavy chain 8, skeletal muscle, perinatal, also known as MYH8, is a human gene.[1]
References
Further reading
- Bober E, Buchberger-Seidl A, Braun T, et al. (1990). "Identification of three developmentally controlled isoforms of human myosin heavy chains.". Eur. J. Biochem. 189 (1): 55–65. PMID 1691980.
- Bober E, Lyons GE, Braun T, et al. (1991). "The muscle regulatory gene, Myf-6, has a biphasic pattern of expression during early mouse development.". J. Cell Biol. 113 (6): 1255–65. PMID 2045411.
- Karsch-Mizrachi I, Feghali R, Shows TB, Leinwand LA (1990). "Generation of a full-length human perinatal myosin heavy-chain-encoding cDNA.". Gene 89 (2): 289–94. PMID 2373371.
- Feghali R, Leinwand LA (1989). "Molecular genetic characterization of a developmentally regulated human perinatal myosin heavy chain.". J. Cell Biol. 108 (5): 1791–7. PMID 2715179.
- Jullian EH, Kelly AM, Pompidou AJ, et al. (1995). "Characterization of a human perinatal myosin heavy-chain transcript.". Eur. J. Biochem. 230 (3): 1001–6. PMID 7601129.
- Soussi-Yanicostas N, Whalen RG, Petit C (1993). "Five skeletal myosin heavy chain genes are organized as a multigene complex in the human genome.". Hum. Mol. Genet. 2 (5): 563–9. PMID 8518795.
- Veugelers M, Bressan M, McDermott DA, et al. (2004). "Mutation of perinatal myosin heavy chain associated with a Carney complex variant.". N. Engl. J. Med. 351 (5): 460–9. doi:. PMID 15282353.
- Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.". Genome Res. 16 (1): 55–65. doi:. PMID 16344560.
- Toydemir RM, Chen H, Proud VK, et al. (2007). "Trismus-pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8.". Am. J. Med. Genet. A 140 (22): 2387–93. doi:. PMID 17041932.
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