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KAL1 wt Allele

Known as: KALIG-1, KMS, HHA 
Human KAL1 wild-type allele is located in the vicinity of Xp22.32 and is approximately 203 kb in length. This allele, which encodes anosmin-1 protein… 
National Institutes of Health

Related topics

Related topics

11 relations
ANOS1 geneCell AdhesionCell MovementHomo sapiens

Papers overview

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Highly Cited
2005
Highly Cited
2005
Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2)
Kallmann syndrome (KAL) combines hypogonadotropic hypogonadism and anosmia. Hypogonadism is due to Gonadotropin Releasing Hormone… 
Highly Cited
2005
Highly Cited
2005
Modulation of multiply scattered coherent light by ultrasonic pulses: an analytical model.
We present an analytical solution for the acousto-optical modulation of multiply scattered light in a medium irradiated with a… 
Review
2003
Review
2003
Genetic disorders of human congenital anomalies of the kidney and urinary tract (CAKUT)
Congenital abnormalities of the kidney and urinary tract, CAKUT are common in humans, occurring at a frequency of approximately 1… 
Highly Cited
2001
Highly Cited
2001
Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization*
OBJECTIVE The association of idiopathic hypogonadotrophic hypogonadism (IHH) with congenital olfactory deficit defines Kallmann's… 
Highly Cited
2001
Highly Cited
2001
The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics.
Kallmann syndrome (KS) consists of congenital, isolated, idiopathic hypogonadotropic hypogonadism (IHH) and anosmia. The gene… 
Review
1996
Review
1996
The neuroradiology of Kallmann's syndrome: a genotypic and phenotypic analysis.
A detailed neurological investigation of patients with Kallmann's syndrome (KS) has been performed in an attempt to relate… 
Highly Cited
1995
Highly Cited
1995
KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human development
Highly Cited
1994
Highly Cited
1994
Expression of the Kallmann syndrome gene in human fetal brain and in the manipulated chick embryo.
Kallmann syndrome is an inherited disorder characterized by an abnormality in olfactory system development. The gene for the X… 
Highly Cited
1993
Highly Cited
1993
Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome.
Kallmann syndrome represents the association of hypogonadotropic hypogonadism with anosmia. Three modes of transmission, X… 
Highly Cited
1989
Highly Cited
1989
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.
Mendelian inherited disorders due to deletions of adjacent genes on a chromosome have been described as "contiguous gene… 
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