ANOS1, anosmin 1

ANOS1, anosmin 1

• Mutations in this gene cause the X-linked Kallmann syndrome. The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N-glycosylated and may have anti-protease activity. [provided by RefSeq, Jul 2008]

• Gene Synonyms (ADMLX, HH1, HHA, KAL, KAL1, KALIG-1, KMS, WFDC19, anosmin-1, Kallmann syndrome interval gene 1, Kallmann syndrome-1 sequence (anosmin-1), WAP four-disulfide core domain 19, adhesion molecule-like X-linked, kallmann syndrome protein,)
• NCBI Gene ID: 3730
• Species: Homo sapiens (Human)
• UNIPROT ID#>>P23352
• 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.

anosmin 1 interacts with:

• anosmin 1
  DEAD-box helicase 42
  laminin B1
  laminin, alpha 1
  laminin, beta 2
  neurocalcin delta
  syndecan 2
  ubiquilin 1
  vir like m6A methyltransferase associated

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.