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Fig. 2 | BMC Genomics

Fig. 2

From: A nonsense mutation in B3GALNT2 is concordant with hydrocephalus in Friesian horses

Fig. 2

SNP genotypes from 60 to 90 Mb on ECA1 for cases (n = 13) and controls (n = 69). Hydrocephalus associated homozygous genotypes are depicted by red, heterozygous genotypes by yellow, normal homozygous genotypes by green and missing genotypes by black. Each column corresponds to one horse, each row corresponds to one SNP. The candidate mutation in B3GALNT2 is part of a region of 1.47 Mb in length (range: 74,897,451–76,370,694) that is shared homozygous by all 13 cases and one control. The region of 1.47 Mb in length is shown in the enlargement, where obligate carriers (dams of cases) are marked with a star

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