Search Phenotypes

Abortion (embryonic lethality), RNF20-related

Charlier et al. (2016): nonsense (stop-gain) p.Lys693∗

OMIA ID: 2038Inheritance: 6Characterised: YesYear: 2016

Ichthyosis, DSP-related

Häfliger et al. (2022) report a Scottish Highland calf with "combined lesions compatible with congenital ichthyosis, alopecia, acantholysis of the tongue and corneal defects associated with a DSP missense variant as the most likely underlying cause."

OMIA ID: 2243Inheritance: 5Characterised: YesYear: 2022

Mannosidosis, beta

Abbitt et al. (1991) reported that bovine beta-mannosidosis, a lysosomal storage disease, is caused by a deficiency of beta-mannosidase. Affected neonatal calves are unable to rise with intention tremors, hidebound skin, slightly domed calvaria, slight prognathism, and narrow palpebral fissures. Their postmortem findings included variable dilatation of the lateral cerebral ventricles, marked pallor and paucity of white matter of the cerebrum a...

OMIA ID: 626Inheritance: 5Characterised: YesYear: 1999

Thrombopathia, RASGRP2-related — Simmental hereditary thrombopathy; bleeding disorder;

On the strength of a clear candidate gene in which mutations cause the same disorder in dogs (OMIA 001003-9615), Boudreaux et al. (2007) reported that this disorder in a Simmental calf is due to a missense mutation (c.701T>C) in the CalDAG-GEFI gene which is now called RASGRP2. Jansen et al. (2013) reported that "Sanger sequencing confirmed that all thrombopathic animals are homozygous for the [same] pertinent amino acid exchange (c.701T &g...

OMIA ID: 2433Inheritance: 5Characterised: YesYear: 2007