Search Phenotypes

Haplotype with homozygous deficiency NH8

No summary available.

OMIA ID: 2202Inheritance: N/ACharacterised: NoYear: N/A

Haplotype with homozygous deficiency OH2, TUBGCP5-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: 2515Inheritance: 5Characterised: YesYear: 2021

Haplotype with homozygous deficiency OH4, LIG3-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: 2516Inheritance: 5Characterised: YesYear: 2021

Haplotype with homozygous deficiency SH1

Häfliger et al. (2021) “report the result of a large-scale reverse genetic screen in the Swiss Simmental population …. We used 115,000 phased SNP data of almost 10 thousand cattle with pedigree data. This revealed evidence for 11 genomic regions … with haplotypes (SH1 to SH11) showing a significant depletion in homozygosity and an allele frequency between 3.2 and 10.6%. For the proposed haplotypes, it was unfortunately not possible to evaluate...

OMIA ID: 2501Inheritance: N/ACharacterised: NoYear: N/A

Haplotype with homozygous deficiency SH10

Häfliger et al. (2021) “report the result of a large-scale reverse genetic screen in the Swiss Simmental population …. We used 115,000 phased SNP data of almost 10 thousand cattle with pedigree data. This revealed evidence for 11 genomic regions … with haplotypes (SH1 to SH11) showing a significant depletion in homozygosity and an allele frequency between 3.2 and 10.6%. For the proposed haplotypes, it was unfortunately not possible to evaluate...

OMIA ID: 2510Inheritance: N/ACharacterised: NoYear: N/A

Haplotype with homozygous deficiency SH11

Häfliger et al. (2021) “report the result of a large-scale reverse genetic screen in the Swiss Simmental population …. We used 115,000 phased SNP data of almost 10 thousand cattle with pedigree data. This revealed evidence for 11 genomic regions … with haplotypes (SH1 to SH11) showing a significant depletion in homozygosity and an allele frequency between 3.2 and 10.6%. For the proposed haplotypes, it was unfortunately not possible to evaluate...

OMIA ID: 2511Inheritance: N/ACharacterised: NoYear: N/A

Haplotype with homozygous deficiency SH2

Häfliger et al. (2021) “report the result of a large-scale reverse genetic screen in the Swiss Simmental population …. We used 115,000 phased SNP data of almost 10 thousand cattle with pedigree data. This revealed evidence for 11 genomic regions … with haplotypes (SH1 to SH11) showing a significant depletion in homozygosity and an allele frequency between 3.2 and 10.6%. For the proposed haplotypes, it was unfortunately not possible to evaluate...

OMIA ID: 2502Inheritance: N/ACharacterised: NoYear: N/A

Haplotype with homozygous deficiency SH3

Häfliger et al. (2021) “report the result of a large-scale reverse genetic screen in the Swiss Simmental population …. We used 115,000 phased SNP data of almost 10 thousand cattle with pedigree data. This revealed evidence for 11 genomic regions … with haplotypes (SH1 to SH11) showing a significant depletion in homozygosity and an allele frequency between 3.2 and 10.6%. For the proposed haplotypes, it was unfortunately not possible to evaluate...

OMIA ID: 2503Inheritance: N/ACharacterised: NoYear: N/A

Haplotype with homozygous deficiency SH4

Häfliger et al. (2021) “report the result of a large-scale reverse genetic screen in the Swiss Simmental population …. We used 115,000 phased SNP data of almost 10 thousand cattle with pedigree data. This revealed evidence for 11 genomic regions … with haplotypes (SH1 to SH11) showing a significant depletion in homozygosity and an allele frequency between 3.2 and 10.6%. For the proposed haplotypes, it was unfortunately not possible to evaluate...

OMIA ID: 2504Inheritance: N/ACharacterised: NoYear: N/A

Haplotype with homozygous deficiency SH5, DIS3-related

Häfliger et al. (2021) “report the result of a large-scale reverse genetic screen in the Swiss Simmental population …. We used 115,000 phased SNP data of almost 10 thousand cattle with pedigree data. This revealed evidence for 11 genomic regions … with haplotypes (SH1 to SH11) showing a significant depletion in homozygosity and an allele frequency between 3.2 and 10.6%. For the proposed haplotypes, it was unfortunately not possible to evaluate...

OMIA ID: 2505Inheritance: 5Characterised: YesYear: 2021

Haplotype with homozygous deficiency SH6

Häfliger et al. (2021) “report the result of a large-scale reverse genetic screen in the Swiss Simmental population …. We used 115,000 phased SNP data of almost 10 thousand cattle with pedigree data. This revealed evidence for 11 genomic regions … with haplotypes (SH1 to SH11) showing a significant depletion in homozygosity and an allele frequency between 3.2 and 10.6%. For the proposed haplotypes, it was unfortunately not possible to evaluate...

OMIA ID: 2506Inheritance: N/ACharacterised: NoYear: N/A

Haplotype with homozygous deficiency SH7

Häfliger et al. (2021) “report the result of a large-scale reverse genetic screen in the Swiss Simmental population …. We used 115,000 phased SNP data of almost 10 thousand cattle with pedigree data. This revealed evidence for 11 genomic regions … with haplotypes (SH1 to SH11) showing a significant depletion in homozygosity and an allele frequency between 3.2 and 10.6%. For the proposed haplotypes, it was unfortunately not possible to evaluate...

OMIA ID: 2507Inheritance: N/ACharacterised: NoYear: N/A

Haplotype with homozygous deficiency SH8, CYP2B6-related

Häfliger et al. (2021) “report the result of a large-scale reverse genetic screen in the Swiss Simmental population …. We used 115,000 phased SNP data of almost 10 thousand cattle with pedigree data. This revealed evidence for 11 genomic regions … with haplotypes (SH1 to SH11) showing a significant depletion in homozygosity and an allele frequency between 3.2 and 10.6%. For the proposed haplotypes, it was unfortunately not possible to evaluate...

OMIA ID: 2508Inheritance: 5Characterised: YesYear: 2021

Haplotype with homozygous deficiency SH9, NUBPL-related

Häfliger et al. (2021) “report the result of a large-scale reverse genetic screen in the Swiss Simmental population …. We used 115,000 phased SNP data of almost 10 thousand cattle with pedigree data. This revealed evidence for 11 genomic regions … with haplotypes (SH1 to SH11) showing a significant depletion in homozygosity and an allele frequency between 3.2 and 10.6%. For the proposed haplotypes, it was unfortunately not possible to evaluate...

OMIA ID: 2509Inheritance: 5Characterised: YesYear: 2021

Haplotype with homozygous deficiency, AA14H3

Jenko et al. (2019): Haplotype AA14H3 was "associated with decreased insemination success rate and a longer interval between insemination and calving."

OMIA ID: 2395Inheritance: 7Characterised: NoYear: N/A