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- NCIT_C97648 IAO_0000115 "Human MYH9 wild-type allele is located in the vicinity of 22q13.1 and is approximately 107 kb in length. This allele, which encodes myosin-9 protein, plays a role in both cytokinesis and cell shape. Mutation of the gene is associated with May-Hegglin anomaly, non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness and non-diabetic end stage renal disease. A chromosomal translocation t(2;22)(p23;q12) of this gene and the ALK gene is associated with anaplastic large cell lymphoma." @default.
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- NCIT_C97648 hasExactSynonym "DFNA17" @default.
- NCIT_C97648 hasExactSynonym "EPSTS" @default.
- NCIT_C97648 hasExactSynonym "FTNS" @default.
- NCIT_C97648 hasExactSynonym "MGC104539" @default.
- NCIT_C97648 hasExactSynonym "MHA" @default.
- NCIT_C97648 hasExactSynonym "MYH9 wt Allele" @default.
- NCIT_C97648 hasExactSynonym "Myosin Heavy Chain 9 wt Allele" @default.
- NCIT_C97648 hasExactSynonym "Myosin, Heavy Chain 9, Non-Muscle Gene" @default.
- NCIT_C97648 hasExactSynonym "Myosin, Heavy Polypeptide 9, Non-Muscle Gene" @default.
- NCIT_C97648 hasExactSynonym "NMHC-II-A" @default.
- NCIT_C97648 hasExactSynonym "NMMHCA" @default.
- NCIT_C97648 hasExactSynonym "Nonmuscle Myosin Heavy Chain II-A Gene" @default.
- NCIT_C97648 hasExactSynonym "RP1-68O2.1" @default.
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- NCIT_C97648 type Class @default.
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- NCIT_C97648 label "MYH9 wt Allele" @default.
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