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Gene : MYH9 Homo sapiens

Name  ? myosin heavy chain 9 Cytological Location  22q12.3
Brief Description  myosin heavy chain 9
description  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]
  • synonyms:
  • OTTHUMG00000030429,
  • NMHC-II-A,
  • uc003apg.4,
  • MHA,
  • NM_002473,
  • DFNA17,
  • nonmuscle myosin heavy chain II-A,
  • FTNS,
  • myosin, heavy polypeptide 9, non-muscle,
  • HGNC:7579,
  • EPSTS,
  • EPSTS,
  • MYH9,
  • DFNA17,
  • NMMHCA,
  • NMMHCA,
  • NMMHC-IIA,
  • NMHC-II-A,
  • FTNS,
  • MATINS,
  • MHA,
  • BDPLT6
  • identifiers:
  • 4627,
  • ENSG00000100345,
  • MYH9

Genome feature

Region: gene ? Length: 106791  
Location: 22:36281277-36388067 reverse strand Cyto location: 22q12.3


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> GO terms.

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

2 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

37 SN Ps

5 Cross References

20 Data Sets

23 Homologues

1 Located Features

90 Rna Seq Results