Variant: rs104894373 

    present in Gene: RDH5;BLOC1S1-RDH5
    present in Chromosome: 12
    Position on Chromosome: 55721908
    Alleles of this Variant: T/G

rs104894373 in RDH5;BLOC1S1-RDH5 gene and Fundus Albipunctatus PMID 10369264 1999 Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus.

PMID 10617778 1999 11-cis retinol dehydrogenase mutations as a major cause of the congenital night-blindness disorder known as fundus albipunctatus.

PMID 11053296 2000 Mutations in the 11-cis retinol dehydrogenase gene in Japanese patients with Fundus albipunctatus.

PMID 25820994 2015 Fundus albipunctatus: review of the literature and report of a novel RDH5 gene mutation affecting the invariant tyrosine (p.Tyr175Phe).

PMID 11078852 2000 The occurrence of Val177Gly has not been reported in the RDH5 gene of fundus albipunctatus.

PMID 11675386 2001 Biochemical defects in 11-cis-retinol dehydrogenase mutants associated with fundus albipunctatus.

PMID 11470705 2001 Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatus.

PMID 28418496 2017 Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families.

PMID 12967826 2003 A novel RDH5 gene mutation in a patient with fundus albipunctatus presenting with macular atrophy and fading white dots.

PMID 11053295 2000 A high association with cone dystrophy in Fundus albipunctatus caused by mutations of the RDH5 gene.

PMID 22736946 2012 Novel mutations in RDH5 cause fundus albipunctatus in two consanguineous Pakistani families.

PMID 12788147 2003 Macular dystrophy in a Japanese family with fundus albipunctatus.

PMID 24603341 2014 exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels.