Search Phenotypes

Haplotype with homozygous deficiency MH2

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: 1828Inheritance: 6Characterised: YesYear: 2013

Haplotype with homozygous deficiency MH3

No summary available.

OMIA ID: 1842Inheritance: 5Characterised: NoYear: N/A

Haplotype with homozygous deficiency MH4

No summary available.

OMIA ID: 1843Inheritance: 5Characterised: NoYear: N/A

Haplotype with homozygous deficiency MH5

No summary available.

OMIA ID: 1844Inheritance: 5Characterised: NoYear: N/A

Haplotype with homozygous deficiency MH6

No summary available.

OMIA ID: 1845Inheritance: 5Characterised: NoYear: N/A

Haplotype with homozygous deficiency MH7

No summary available.

OMIA ID: 1846Inheritance: 5Characterised: NoYear: N/A

Haplotype with homozygous deficiency MH8

No summary available.

OMIA ID: 1847Inheritance: 5Characterised: NoYear: N/A

Haplotype with homozygous deficiency MH9

No summary available.

OMIA ID: 1848Inheritance: 5Characterised: NoYear: N/A

Haplotype with homozygous deficiency NH1

No summary available.

OMIA ID: 1851Inheritance: 5Characterised: NoYear: N/A

Haplotype with homozygous deficiency NH2

No summary available.

OMIA ID: 1852Inheritance: 5Characterised: NoYear: N/A

Haplotype with homozygous deficiency NH3

No summary available.

OMIA ID: 1853Inheritance: 5Characterised: NoYear: N/A

Haplotype with homozygous deficiency NH4

No summary available.

OMIA ID: 1854Inheritance: 5Characterised: NoYear: N/A

Haplotype with homozygous deficiency NH5

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: 1829Inheritance: 5Characterised: NoYear: N/A

Haplotype with homozygous deficiency NH6

No summary available.

OMIA ID: 1855Inheritance: 5Characterised: NoYear: N/A

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