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TBC1D7, TBC1 domain family member 7

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TBC1D7, TBC1 domain family member 7

  • This gene encodes a member of the TBC-domain containing protein family. The encoded protein functions as a subunit of the tuberous sclerosis TSC1-TSC2 complex which plays a role in the regulation of cellular growth and differentiation. Mutations in this gene have been associated with autosomal recessive megalencephaly. Alternative splicing results in multiple transcript variants. Naturally occurring readthrough transcription occurs between this locus and downstream LOC100130357. [provided by RefSeq, Jan 2016]

  • Gene Synonyms (TBC1 domain family member 7, TS complex subunit 3, cell migration-inducing protein 23, MGCPH, PIG51, TBC7,)
  • NCBI Gene ID: 51256
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q5JPB9
    UNIPROT ID#>>U3KPY5
    UNIPROT ID#>>A0A024QZX0
    UNIPROT ID#>>A0A024R011
    UNIPROT ID#>>Q9P0N9
  • 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.

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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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