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TAZ, tafazzin

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TAZ, tafazzin

  • This gene encodes a protein that is expressed at high levels in cardiac and skeletal muscle. Mutations in this gene have been associated with a number of clinical disorders including Barth syndrome, dilated cardiomyopathy (DCM), hypertrophic DCM, endocardial fibroelastosis, and left ventricular noncompaction (LVNC). Multiple transcript variants encoding different isoforms have been described. A long form and a short form of each of these isoforms is produced; the short form lacks a hydrophobic leader sequence and may exist as a cytoplasmic protein rather than being membrane-bound. Other alternatively spliced transcripts have been described but the full-length nature of all these transcripts is not known. [provided by RefSeq, Jul 2008]

  • Gene Synonyms (tafazzin, protein G4.5, BTHS, CMD3A, EFE, EFE2, G4.5, LVNCX, Taz1,)
  • NCBI Gene ID: 6901
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q16635
    UNIPROT ID#>>A0A0S2Z4K0
    UNIPROT ID#>>A0A0S2Z4K9
    UNIPROT ID#>>A0A0S2Z4F4
    UNIPROT ID#>>A6XNE1
    UNIPROT ID#>>A0A0S2Z4E6
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

tafazzin interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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