Search Phenotypes

Abortion (embryonic lethality), RABGGTB-related

Charlier et al. (2016): missense p.Tyr195Cys

OMIA ID: 2037Inheritance: 6Characterised: YesYear: 2016

Achromatopsia-3, CNGB3-related

Häfliger et al. (2021) "characterize the phenotype and the genetic aetiology of a recessive form of congenital day-blindness observed in several cases of purebred Original Braunvieh cattle. ... Achromatopsia is a monogenic Mendelian disease characterized by the loss of cone photoreceptor function resulting in day-blindness, total color-blindness, and decreased central visual acuity."

OMIA ID: 1365Inheritance: Häfliger et al. (2021) "available pedigree records of all 12 cases were analy...Characterised: YesYear: 2021

Coat colour, roan

By cloning and sequencing a very likely comparative positional candidate gene (see the Genetic mapping section above), Seitz et al. (1999) reported that a missense mutation at 654 bp (amino acid 193, Ala>Asp) in the mast cell growth factor (MGF) locus is responsible for the roan phenotype in Belgian Blue and Shorthorn cattle (Mohammad Shariflou. The MGF gene is now called KITLG (10/11/2006; FN 15/9/2012)

OMIA ID: 1216Inheritance: 4Characterised: YesYear: 1999

Gangliosidosis, GM2, type I (B variant)

Eager et al. (2025): "Whole-genome sequencing of an affected calf identified a homozygous frameshift variant in the HEXA gene (NC_037337.1:g.19269480_19269481delinsGGAGT, NM_001075164.2: c.(834_835delinsACTCC)), absent from 18 control genomes and 1842 individuals in the 1000 Bull Genomes Project. The variant was confirmed in homozygous form in all four affected animals by Sanger sequencing and meets multiple criteria for pathogenicity."

OMIA ID: 1461Inheritance: 5Characterised: YesYear: 2025

Haplotype with homozygous deficiency HH4 — Haplotype HH4

For eight of the nine haplotypes with a significant effect on calving rate (see Mapping section), Fritz et al. (2013) searched for causal mutations via whole-genome sequence data from 25 Holstein, 11 Montbéliarde and nine Normande bulls which had made major contributions to their breed. Specifically, they filtered "for mutations that were (a) located at+or –6 Mb from the detected haplotype (b) carried in the heterozygous state by the carrier b...

OMIA ID: 1826Inheritance: 6Characterised: YesYear: 2013

Lethality, SOWAHB-related

Bourneuf et al. (2017) detected SOWAHB g.93487577G>T; p.Q379K as a de novo recessive potentially lethal mutation from an analysis of whole-genome-sequence of a Charolais AI bull. No information was provided on the descendants of this bull.

OMIA ID: 2258Inheritance: 5Characterised: YesYear: 2017

Muscular hypertrophy (double muscling) — Double muscling; “culón”; horse rump

The double-muscle trait in cattle is characterised by an increase in muscle mass of approx 20%, resulting in substantially higher meat yield, a higher proportion of expensive cuts of meat, and lean and very tender meat, for which a substantial premium is paid. The trait is autosomal recessive, and the locus has been given the symbol mh. It occurs at such a high frequency in Piedmontese and Belgian Blue cattle that it is characteristic of these...

OMIA ID: 683Inheritance: 1Characterised: YesYear: 1997

Rhizomelic chondrodysplasia punctata, PEX7-related — bulldog calves

No summary available.

OMIA ID: 2973Inheritance: N/ACharacterised: NoYear: N/A