Search Phenotypes

Anhidrotic ectodermal dysplasia, EDAR-related

Bourneuf et al. (2017): a de novo likely causal variant in Charolais is single-base insertion in EDAR, resulting in a frameshift variant g.44462236_44462237insC; p.P161RfsX97

OMIA ID: 2128Inheritance: 5Characterised: YesYear: 2017

Coat colour, extension — Black/red coat colour; Haplotype HBR; Haplotype HHR

For information relating to Bos indicus cattle see: OMIA 001199-9915 : Coat colour, extension in Bos indicus

OMIA ID: 1199Inheritance: As summarised by Lawlor et al. (2014), "Dominant inheritance of black over re...Characterised: YesYear: 1995

Goitre, familial

The causative mutation for this disorder was discovered via the candidate gene approach. Tassi et al. (1984) reported a 10-15-fold decrease in the concentration of TG mRNA in affected cattle; Ricketts et al. (1985) reported the use of S1 nuclease assays and electron microscopy to narrow down the location of the mutation to the junction of exon 9 and intron 9; and Ricketts et al. (1987) reported the use of cloning and sequencing of genomic DNA ...

OMIA ID: 424Inheritance: 1Characterised: YesYear: 1987

Haplotype with homozygous deficiency BH24, CPT1C-related

Häfliger et al. (2021) investigated “the two Braunvieh populations reared in Switzerland, the dairy Brown Swiss (BS) and the dual-purpose Original Braunvieh (OB). We performed a genome-wide analysis of array data of trios (sire, dam, and offspring) from the routine genomic selection to identify candidate regions showing missing homozygosity and phenotypic associations with five fertility, ten birth, and nine growth-related traits. In addition,...

OMIA ID: 2519Inheritance: 5Characterised: YesYear: 2021

Haplotype with homozygous deficiency HH25, RIOX1-related

No summary available.

OMIA ID: 2547Inheritance: Häfliger et al. (2022) reported a 75% deficiency of homozygotes for this hapl...Characterised: YesYear: 2022

Neuronal ceroid lipofuscinosis, 3 — delayed-onset retinal degeneration

Reith et al. (2024): "Whole-genome sequencing (WGS) of 7 blind cattle and 9 unaffected relatives revealed a 1-bp frameshift deletion in ceroid lipofuscinosis neuronal 3 (CLN3; chr25 g.26043843del) for which the blind cattle were homozygous and their parents heterozygous. The identified variant in exon 16 of 17 is predicted to truncate the encoded protein (p. Pro369Argfs*8) ... ."

OMIA ID: 2432Inheritance: Reith et al. (2024): "All blind [Hereford] cattle shared a common ancestor th...Characterised: YesYear: 2024

Syndactyly — Mule foot disease; mulefoot; Haplotype HHM

Syndactyly has been reported in many breeds of cattle in many countries. Most of the documentation, however, concerns its occurrence in US Holsteins, where, as a result of the siring of more than 60,000 calves by a bull who was subsequently shown to be a carrier, the disorder attracted considerable attention (Anon., 1967). The possibility that artificial selection favouring heterozygotes may have contributed to the unacceptably high frequency ...

OMIA ID: 963Inheritance: 5Characterised: YesYear: 2006