ALX1, ALX homeobox 1

ALX1, ALX homeobox 1

• The specific function of this gene has yet to be determined in humans; however, in rodents, it is necessary for survival of the forebrain mesenchyme and may also be involved in development of the cervix. Mutations in the mouse gene lead to neural tube defects such as acrania and meroanencephaly. [provided by RefSeq, Jul 2008]

• Gene Synonyms (ALX homeobox protein 1, CART-1, cartilage paired-class homeoprotein 1, epididymis luminal protein 23, CART1, FND3, HEL23,)
• NCBI Gene ID: 8092
• Species: Homo sapiens (Human)
• UNIPROT ID#>>V9HWA7
  UNIPROT ID#>>Q15699
• 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.

ALX homeobox 1 interacts with:

• ALX homeobox 4
  chloride intracellular channel 3
  importin 13
  keratin associated protein 4-4
  lysine acetyltransferase 5
  olfactory receptor family 52 subfamily L member 1
  parkin coregulated like
  RNA binding motif protein 45
  steroid receptor RNA activator 1
  urocanate hydratase 1
  zinc finger and BTB domain containing 38
  zinc finger protein 300

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.