myh9 Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description myosin, heavy chain 9, non-muscle|This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq, Dec 2011] (NCBI Entrez Gene Database, 4627)
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Genes

11 genes co-occuring with the biological term myh9 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
ALK anaplastic lymphoma receptor tyrosine kinase
APOL1 apolipoprotein L, 1
FBLN1 fibulin 1
ITGAL integrin, alpha L (antigen CD11A (p180), lymphocyte function-associated antigen 1; alpha polypeptide)
MYH6 myosin, heavy chain 6, cardiac muscle, alpha
MYH9 myosin, heavy chain 9, non-muscle
NUCLEOLIN nucleolin multifunctional protein
OVGP1 oviductal glycoprotein 1, 120kDa
USP2 ubiquitin specific peptidase 2
VEGFA vascular endothelial growth factor A
WASF2 WAS protein family, member 2