C75620Level 5
ANOS1 wt Allele
**Semantic type:** Gene or Genome
**Definition:** Human ANOS1 wild-type allele is located in the vicinity of Xp22.31 and is approximately 203 kb in length. This allele, which encodes anosmin-1 protein, may be involved in the regulation of both cell adhesion and proteolysis. Mutations in the gene are associated with Kallmann Syndrome 1.
**Synonyms:** - ADMLX - Adhesion Molecule-Like, X-Linked Gene - Anosmin 1 wt Allele - HH1 - HHA - KAL - KAL1 - KALIG-1 - KMS - Kallmann Syndrome 1 Sequence Gene - Kallmann Syndrome Interval Gene 1 - Kallmann Syndrome-1 Sequence (Anosmin-1) Gene - WFDC19
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Cross-system equivalences0
No cross-system equivalences mapped for this node.