MYH9 wt Allele

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. (NCI Thesaurus)

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MYH9 Gene

This gene is involved in both cytoskeleton modeling and cytokinesis.

MYH2 wt Allele

Human MYH2 wild-type allele is located in the vicinity of 17p13.1 and is approximately 85 kb in length. This allele, which encodes…

MYH2 Gene

This gene is involved in skeletal muscle contraction.

MYH11 wt Allele

Human MYH11 wild-type allele is located in the vicinity of 16p13.11 and is approximately 154 kb in length. This allele, which encodes…

MYH11 Gene

This gene plays a regulatory role in muscle contraction and the required ATP hydrolysis.

MYH1 wt Allele

Human MYH1 wild-type allele is located in the vicinity of 17p13.1 and is approximately 26 kb in length. This allele, which encodes…