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TMEM237, transmembrane protein 237

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TMEM237, transmembrane protein 237

  • The protein encoded by this gene is a tetraspanin protein that is thought to be involved in WNT signaling. Defects in this gene are a cause of Joubert syndrome-14. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]

  • Gene Synonyms (transmembrane protein 237, amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 4, amyotrophic lateral sclerosis 2 chromosomal region candidate gene 4 protein, ALS2CR4, JBTS14,)
  • NCBI Gene ID: 65062
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q96Q45
  • 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 237 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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