" /> TPM1 wt Allele - CISMeF





Preferred Label : TPM1 wt Allele;

NCIt synonyms : Cardiomyopathy, Hypertrophic 3 Gene; HTM-alpha; CMH3; LVNC9; C15orf13; CMD1Y; TMSA; Tropomyosin 1 (Alpha) wt Allele; Chromosome 15 Open Reading Frame 13 Gene;

NCIt definition : Human TPM1 wild-type allele is located in the vicinity of 15q22.1 and is approximately 29 kb in length. This allele, which encodes tropomyosin alpha-1 chain protein, is involved in the regulation of muscle contraction. Mutation of the gene is associated with left ventricular non-compaction 9 and cardiomyopathy types familial hypertrophic 3 and dilated 1Y.;

GenBank Accession Number : AB209041;

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04/12/2022


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