Search Phenotypes

Cardiomyopathy, dilated — Bovine hereditary cardiomyopathy; Bovine dilated cardiomyopathy

In a segregation analysis of data from a breeding herd, Dolf et al. (1998) provided convincing evidence of autosomal recessive inheritance.

OMIA ID: 162Inheritance: 5Characterised: YesYear: 2011

Cleft palate, MYH3-related

Vaiman et al. (2022): "The genome of two affected animals was sequenced ... . ... two fully linked mutations in exon 24 of the MYH3 (myosin heavy chain) gene were detected: a 1-bp non-synonymous substitution (BTA19:g.29609623A>G) and a 11-bp frameshift deletion (BTA19:g.29609605-29609615del). These two mutations were specific to the Limousine breed, with an estimated allele frequency of 2.4% and are predicted to be deleterious. ... mRNA and...

OMIA ID: 2590Inheritance: Vaiman et al. (2022): "Based on pedigree analysis, occurrence of cleft palate...Characterised: YesYear: 2022

Complex vertebral malformation — Haplotype HHC

Complex vertebral malformation is an inherited syndrome in Holstein-Friesian cattle. CVM has been reported in aborted, premature born, stillborn and neonatal calves. Affected calves have a reduced weight, a misshapen backbone and tendon contractions in the legs. Several other malformations including heart malformations are associated with this syndrome. A DNA test is available in Denmark and the Netherlands. [Imke Tammen: 26 Jan 2002] From a s...

OMIA ID: 1340Inheritance: 5Characterised: YesYear: 2006

Hypotrichosis, KRT71-related

Jacinto et al. (2021): "Protein-coding exons of six positional candidate genes with known hair or hair follicle function were re-sequenced. This revealed a protein-changing variant in the KRT71 gene that encodes a type II keratin specifically expressed in the IRS of the hair follicle (c.281delTGTGCCCA; p.Met94AsnfsX14)." This variant was previously reported by Markey et al. (2010).

OMIA ID: 2114Inheritance: N/ACharacterised: YesYear: 2010

Ichthyosis, ABCA12-related

In the words of Charlier et al. (2008): "a missense mutation in exon 39 (A5804G) resulting in an H1935R substitution in the fourth extracellular loop". The His (normal) form of the peptide is conserved in all vertebrates sequenced to date. (FN 080330) Whole-genome sequencing of the affected Shorthorn calf described by O'Rourke et al. (2017), and subsequent checking for deleterious variants in functional candidate genes, enabled Woolley et al. ...

OMIA ID: 2238Inheritance: 5Characterised: YesYear: 2008

Niemann-Pick disease, type C1

Woolley et al. (2020) report clinical signs, pathology, fibroblast cell culture analysis and identification of a likely disease causing mutation for Niemann-Pick type C disease in Australian Angus/Angus-cross calves.

OMIA ID: 725Inheritance: 5Characterised: YesYear: 2020