Search Phenotypes

Coat colour, agouti

No summary available.

OMIA ID: 201Inheritance: N/ACharacterised: YesYear: 2006

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

Coat colour, white spotting, KIT-related — Hereford pattern or white headed, as well as spotting

Fontanesi  et al. (2010): "[V]ariation in the white spotting in several cattle breeds is largely influenced by the multiple allelic series at the S locus, which includes at least four alleles (Olson 1999): SH (Hereford pattern), SP (Pinzgauer pattern or lineback), S+ (non-spotted) and s (spotting pattern). The SH allele gives white face, belly, feet and tail, often with a white stripe over the shoulder when homozygous. The SP allele gives pigm...

OMIA ID: 1737Inheritance: The white-headed phenotype is inherited in a dominant mode of inheritance.Characterised: YesYear: 2020

Haplotype with homozygous deficiency NH7, CAD-related

Mesbah-Uddin et al. (2019) reported a likely causal variant as a "missense mutation CAD g.72399397T>C (p.Tyr452Cys)"

OMIA ID: 2201Inheritance: 6Characterised: YesYear: 2019

Haplotype with homozygous deficiency, RFC5-related

Besnard et al. (2023) "present a data-mining framework designed to detect recessive defects in livestock that have been previously missed due to a lack of specific signs, incomplete penetrance, or incomplete linkage disequilibrium. This approach leverages the massive data generated by genomic selection. Its basic principle is to compare the observed and expected numbers of homozygotes for sliding haplotypes in animals with different life histo...

OMIA ID: 2873Inheritance: 11Characterised: YesYear: 2023

Osteogenesis imperfecta, type II, COL1A1-related

Bourneuf et al. (2017): a de novo likely causal variant is COL1A1 p.1049_1050delinsS in Fleckvieh Petersen et al. (2019): "Whole-genome sequencing revealed the presence of a missense mutation in the alpha 1 chain of collagen Type I (COL1A1), for which both calves were heterozygous. The variant resulted in the substitution of a glycine residue with serine in the triple helical domain of the protein; in this region, glycine normally occupies eve...

OMIA ID: 2127Inheritance: 3Characterised: YesYear: 2017

Retinitis pigmentosa 1

Michot et al. (2016): "a one base pair insertion (Chr14: g.23995411_23995412insA) that affects the retinitis pigmentosa-1 gene (RP1) . . . [and] is predicted to cause a frameshift at codon 791 and to terminate the protein 13 amino acids later (p. R791KfsX13)".

OMIA ID: 2029Inheritance: 5Characterised: YesYear: 2016