C19orf12, chromosome 19 open reading frame 12

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 »

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:

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.