| Entrez gene ID | | 3730 |
| Official gene symbol | | KAL1 |
| Full name | | Kallmann syndrome 1 sequence |
| Aliases | | ,ADMLX,HHA,KAL,KALIG-1,KMS, |
| Gene summary | | 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] |
| Location | | Chromosome: X Locus: Xp22.32 |
| Gene position | | 8700227 - 8496915 Map Viewer |
| Gene orientation | | minus |
| Gene size | | 203313 bp |
| Gene sequence |
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| OMIM ID | | 308700 |