KAL1

GENE INFORMATION

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Gene name

KAL1 (HGNC Symbol)

Synonyms

ADMLX, KAL, KALIG-1, WFDC19

Description

Kallmann syndrome 1 sequence (HGNC Symbol)

Entrez 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, Jul 2008]

Chromosome

X

Cytoband

p22.31

Chromosome location (bp)

8496915 - 8700227

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000011201 (version 75.37)

Entrez gene

3730

UniProt

P23352 (UniProt - Evidence at protein level)

neXtProt

NX_P23352

Antibodypedia

KAL1 antibodies
 

PROTEIN VIEW

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KAL1-001
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

KAL1-001 ENSP00000262648
ENST00000262648
P23352
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