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QuickView for Tpm-2;jsessionid=CE67D50936C7832BA659B5B0F1021DF1;jsessionid=A8D37E21CA3D1ED014559676710627C1;jsessionid=942CCD861DAD2ACDBE8F980D2C62B594;jsessionid=2282B2B4C117B787088A31879E0ADFE6 (gene)


Gene Symbol:
TPM2 Homo sapiens Homo sapiens
Full name:
tropomyosin 2
Synonyms:
AMCD1, DA1, DA2B, HEL-S-273, NEM4, TMSB, tropomyosin beta chain, epididymis secretory protein Li 273, nemaline myopathy type 4, tropomyosin 2 (beta)
Genomic Location:
Chr 9: 35671990-35680053
Description:
This gene encodes beta-tropomyosin, a member of the actin filament binding protein family, and mainly expressed in slow, type 1 muscle fibers. Mutations in this gene can alter the expression of other sarcomeric tropomyosin proteins, and cause cap disease, nemaline myopathy and distal arthrogryposis syndromes. Alternatively spliced transcript varian...
Orthologs:
Mus musculus Rattus norvegicus Macaca mulatta Danio rerio Pan troglodytes Canis lupus familiaris Bos taurus
External Links:
Entrez Gene
Transcription Factor
Binding Sites:
Cytogenetic Map:
chr 9
9p13.3