Search Phenotypes

Skeletal dysplasia, FGD3-related

Takasuga et al. (2015): "To search for candidate causative variations for skeletal dysplasia and/or CW-3, three sires segregating the CW-3 QTL ... , three non-Q homozygous sires ... , and a Q-homozygous steer ... were subjected to targeted resequencing ... . The 3.3-Mb CW-3 region contained 910 candidate QTNs (858 SNPs and 52 indels), including four non-synonymous and five synonymous SNPs. ... . Non-synonymous SNPs were located in FGD3 ... and...

OMIA ID: 2625Inheritance: 4Characterised: YesYear: 2015