Search Phenotypes

Short spine

No summary available.

OMIA ID: 911Inheritance: 5Characterised: NoYear: N/A

Shoulder and hip luxation

No summary available.

OMIA ID: 2801Inheritance: N/ACharacterised: NoYear: N/A

Situs inversus

No summary available.

OMIA ID: 1102Inheritance: N/ACharacterised: NoYear: N/A

Skeletal deformity

No summary available.

OMIA ID: 917Inheritance: N/ACharacterised: NoYear: N/A

Skeletal dysplasia, FGD3-related

Takasuga et al. (2015): "To search for candidate causative variations for skeletal dysplasia and/or CW-3, three sires segregating the CW-3 QTL ... , three non-Q homozygous sires ... , and a Q-homozygous steer ... were subjected to targeted resequencing ... . The 3.3-Mb CW-3 region contained 910 candidate QTNs (858 SNPs and 52 indels), including four non-synonymous and five synonymous SNPs. ... . Non-synonymous SNPs were located in FGD3 ... and...

OMIA ID: 2625Inheritance: 4Characterised: YesYear: 2015

Skeletal-cardio-enteric dysplasia, MAP2K2-related — skeletal-cardio-enteric dysplasia

Jacinto et al. (2021) characterized "the pathological phenotype of a Romagnola stillborn calf with skeletal-cardio-enteric dysplasia and ... [identified] a genetic cause by whole-genome sequencing (WGS)."

OMIA ID: 2381Inheritance: 9Characterised: YesYear: 2021

Skin defect

No summary available.

OMIA ID: 919Inheritance: N/ACharacterised: NoYear: N/A

Slick hair

This single-locus autosomal dominant trait confers increased thermotolerance within the breeds in which it originated (Senepol and Carora; Olsen et al., 2003) and also within Hosteins, into which it was introgressed (Dikmen et al., 2008; 2014). In the USA, FDA determined in March 2022 that beef cattle with a genome edit to the PRLR gene and their offspring do not raise any safety concerns. "Based on the safety of consumption of meat from conve...

OMIA ID: 1372Inheritance: Olson et al. (2003) reported "a major gene (designated as the slick hair gene...Characterised: YesYear: 2014

Smooth tongue — epitheliogenesis imperfecta linguae

No summary available.

OMIA ID: 922Inheritance: N/ACharacterised: NoYear: N/A

Spasms, congenital, lethal

No summary available.

OMIA ID: 927Inheritance: 6Characterised: NoYear: N/A

Spastic lameness (redundant)

No summary available.

OMIA ID: 926Inheritance: N/ACharacterised: NoYear: N/A

Spastic paresis — posterior paralysis; hind-limb paralysis

In an imaginative approach to investigating an intractable disorder, Pariset et al. (2013) compared gene expression in the most likely candidate tissue (the spinal cord from C6 to L6) between affected and normal animals, using RNA from two pools (of 4 affecteds and 4 normals) on a 15k cDNA expression array that includes cDNA from a bovine brain library and a bovine monocyte library. The 268 differentially expressed genes suggested involvement ...

OMIA ID: 928Inheritance: Leipold et al. (1967) concluded that the "pattern of occurrence suggested rec...Characterised: NoYear: N/A

Spastic syndrome — also called inherited periodic spasticity, IPS

No summary available.

OMIA ID: 929Inheritance: 10Characterised: NoYear: N/A

Sperm defect

No summary available.

OMIA ID: 930Inheritance: N/ACharacterised: NoYear: N/A

Sperm, dag defect of

No summary available.

OMIA ID: 932Inheritance: N/ACharacterised: NoYear: N/A