BioProject

Background: Variants in the KIT gene are responsible for completely white or white spotting phenotypes in many different species. More...

Background: Variants in the KIT gene are responsible for completely white or white spotting phenotypes in many different species. To the authors’ knowledge there are currently 22 defined equine KIT variants that lead to a reduced number of melanocytes. The resulting coat colour phenotypes range from the completely dominant white horses to just a slight increase in the quantitative trait white markings. The known equine KIT variants are responsible for the allele series termed W1 to W201-5, in addition to the sabino-1 (SB1)6 and tobiano (TO)7 alleles. Own analysis: We sequenced the genome of an Icelandic horse with a striking white spotted phenotype (Fig. 1). The horse was born out of solid-coloured parents. We obtained xxx 2 x 125 bp read-pairs on an illumina Hiseq2500, of which yyy read-(pairs) mapped to the EquCab 2 reference genome yielding an 11.1x average genome coverage. The sequence data were submitted to the European Nucleotide Archive with the accession number ????. We analysed the genome sequence for coding variants in the functional candidate genes EDNRB8, KIT, MITF9, and PAX35,9 (Table S1). The horse did not carry any obvious functional variants in EDNRB, MITF, or PAX3. However, we noticed a heterozygous deletion of a single nucleotide in exon 17 of the KIT gene (chr3:77,735,488delG, c.2369delC, p.A790Efs*20). This frameshift variant is predicted to result in either nonsense mediated decay of the mutant transcript or the expression of a KIT protein with a truncated intracellular tyrosine kinase domain. We confirmed this variant by Sanger sequencing. Less...