ANOS1

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]

Description

anosmin 1

Protein family

Disease related genes, Mapped to UniProt SWISS-PROT, Predicted secreted proteins, Protein evidence (Ezkurdia et al 2014), Protein evidence (Kim et al 2014)

Chromosome

X:p22.31 (8528874 - 8732187)

Ensembl ID

ENSG00000011201  (ver. 84.38)

Orthologs

-

UniProt

P23352

neXtProt

NX_P23352

Human splice variants