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TMEM38B, transmembrane protein 38B

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TMEM38B, transmembrane protein 38B

  • This gene encodes an intracellular monovalent cation channel that functions in maintenance of intracellular calcium release. Mutations in this gene may be associated with autosomal recessive osteogenesis. [provided by RefSeq, Oct 2012]

  • Gene Synonyms (trimeric intracellular cation channel type B, C9orf87, D4Ertd89e, OI14, TRIC-B, TRICB, bA219P18.1,)
  • NCBI Gene ID: 55151
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A0A0MRS4
    UNIPROT ID#>>Q9NVV0
  • 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.

transmembrane protein 38B 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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