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C12orf57, chromosome 12 open reading frame 57

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C12orf57, chromosome 12 open reading frame 57

  • This gene is ubiquitously expressed in human tissues. It is required for development of the human corpus callosum. Mutations in this gene are associated with Temtamy syndrome (TEMTYS). Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]

  • Gene Synonyms (C10, GRCC10, protein C10, gene rich cluster C10, likely ortholog of mouse gene rich cluster, C10,)
  • NCBI Gene ID: 113246
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>U3KQ85
    UNIPROT ID#>>F5GXW5
    UNIPROT ID#>>Q99622
  • 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.

chromosome 12 open reading frame 57 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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