anosmin 1
Alias
ADMLX | HH1 | HHA | KAL | KAL1 | KALIG-1 | KMS | WFDC19
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].