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C19orf12, chromosome 19 open reading frame 12

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C19orf12, chromosome 19 open reading frame 12

  • This gene encodes a small transmembrane protein. Mutations in this gene are a cause of neurodegeneration with brain iron accumulation-4 (NBIA4), but the specific function of the encoded protein is unknown. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]

  • Gene Synonyms (protein C19orf12, membrane protein-associated neurodegeneration, neurodegeneration with brain iron accumulation 3, MPAN, NBIA3, NBIA4, SPG43,)
  • NCBI Gene ID: 83636
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q9NSK7
  • 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 19 open reading frame 12 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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