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Gene information for KAL1 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID3730
Official gene symbolKAL1
Full nameKallmann syndrome 1 sequence
Aliases,ADMLX,HHA,KAL,KALIG-1,KMS,
Gene summaryMutations 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]
LocationChromosome: X   Locus: Xp22.32
Gene position8700227 - 8496915  Map Viewer
Gene orientationminus
Gene size203313 bp
Gene sequence
OMIM ID308700