MYH9
protein-coding gene in the species Homo sapiens
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MYH9
Summary
MYH9 is a gene[1].
Key Facts
- MYH9's instance of is recorded as gene[2].
- MYH9 is a type of protein-coding gene[3].
- MYH9's HomoloGene ID is recorded as 129835[4].
- MYH9's genomic start is recorded as 36677327[5].
- MYH9's genomic start is recorded as 36281280[6].
- MYH9's genomic end is recorded as 36784063[7].
- MYH9's genomic end is recorded as 36388010[8].
- MYH9's ortholog is recorded as Myh9[9].
- MYH9's ortholog is recorded as Myh9[10].
- MYH9's ortholog is recorded as myh9a[11].
- MYH9's ortholog is recorded as nmy-1[12].
- MYH9's ortholog is recorded as zip[13].
- MYH9's encodes is recorded as Myosin heavy chain 9[14].
- MYH9's encodes is recorded as MYH9 protein[15].
- MYH9's encodes is recorded as Myosin, heavy polypeptide 9, non-muscle, isoform CRA_a[16].
- MYH9's encodes is recorded as Myosin-9[17].
- MYH9's found in taxon is recorded as Homo sapiens[18].
- MYH9's chromosome is recorded as human chromosome 22[19].
- MYH9's genetic association is recorded as autosomal dominant nonsyndromic deafness 17[20].
- MYH9's genetic association is recorded as MYH9-related disorder[21].
- MYH9's strand orientation is recorded as reverse strand[22].
- MYH9's exact match is recorded as http://identifiers.org/ncbigene/4627[23].
- MYH9's cytogenetic location is recorded as 22q12.3[24].
- MYH9's expressed in is recorded as ascending aorta[25].
- MYH9's expressed in is recorded as stromal cell of endometrium[26].