Variant: rs1555904596

present in Gene: ANOS1 present in Chromosome: X Position on Chromosome: 8731936 Alleles of this Variant: -/AGCAGCCGCGC

rs1555904596 in ANOS1 gene and Dysmorphic features PMID 11390716 2001 Multicystic dysplastic kidney and Kallmann's syndrome: a new association?

PMID 10340754 1999 Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: implications for the developmental anomalies of X chromosome-linked Kallmann syndrome.

PMID 1913827 1991 The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules.

PMID 7820942 1994 Unilateral renal aplasia in X-linked Kallmann's syndrome.

PMID 25300141 2014 The adhesion molecule anosmin-1 in neurology: Kallmann syndrome and beyond.

PMID 15471890 2004 The product of X-linked Kallmann's syndrome gene (KAL1) affects the migratory activity of gonadotropin-releasing hormone (GnRH)-producing neurons.

PMID 1922361 1991 A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules.

rs1555904596 in ANOS1 gene and Multiple congenital anomalies PMID 11390716 2001 Multicystic dysplastic kidney and Kallmann's syndrome: a new association?

PMID 1922361 1991 A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules.

PMID 10340754 1999 Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: implications for the developmental anomalies of X chromosome-linked Kallmann syndrome.

PMID 25300141 2014 The adhesion molecule anosmin-1 in neurology: Kallmann syndrome and beyond.

PMID 1913827 1991 The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules.

PMID 15471890 2004 The product of X-linked Kallmann's syndrome gene (KAL1) affects the migratory activity of gonadotropin-releasing hormone (GnRH)-producing neurons.

PMID 7820942 1994 Unilateral renal aplasia in X-linked Kallmann's syndrome.