VH Harry P - DEU 361199175

Production & Efficiency

Trait Index 80 100 120
Production 105
Milk kg 91
Fat, kg 103
Fat, % 110
Protein kg 101
Protein % 118
Persistency 102
Growth 92
Daily carcass gain 94
Carcass conformation score 92
Saved feed 77
Maintenance efficiency 92
Metabolic efficiency 85

NAV proof run date: 03-12-2024 Reliability 99 % Number of daughters: 6422

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 91 -295.3 11488
Fat kg, 305 days 103 3.7 470
Fat %, 305 days 110 0.16 4.1
Protein kg, 305 days 101 1.0 402
Protein %, 305 days 118 0.13 3.5

NAV proof run date: 03-12-2024 Reliability 99 % Number of daughters: 6422

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 109
Interval from calving to first insemination (cows) 112
Interval from first to last insemination (heifers) 121
Interval from first to last insemination (cows) 106
Number of inseminations (heifers) 120
Number of inseminations (cows) 105
Calving sire 106
Calving maternal 100
Udder health 102
General health 105
Longevity 102
Hoof health 106
Sole Ulcer 101
Sole Hemorrhage 104
Heel Horn Erosion 100
Digital dermatitis + Interdigital Dermatitis 117
Verrucose dermatitis + Interdigital Hyperplasia 106
Double sole + White line separation 112
Cork screw claw 110
Youngstock survival 108

NAV proof run date: 03-12-2024 Reliability 99 % Number of daughters: 6334

Functional

Trait Index 80 100 120
Milkability 110
Temperament 101

NAV proof run date: 03-12-2024 Reliability 96 % Number of daughters: 2399

Conformation

Trait Index 80 100 120
Frame 103
Stature 102 Short Tall
Body depth 107 Shallow Deep
Chest width 99 Narrow Wide
Rib structure 98 Coarse Angular
Top line 87 Weak Strong
Rump width 103 Narrow pins Wide pins
Rump angle 94 High pins Low pins
Feet & legs 109
Rear legs, side view 89 Straight Sickled
Rear legs, back rear view 115 Toes out Parallel, bow-legged
Foot angle 90 Low Steep
Bone quality 105 Coarse Fine and thin
Hock quality 113 Filled Dry
Udder 93
Fore udder attachment 98 Loose Strong
Rear udder height 99 Low High
Rear udder width 99 Narrow Wide
Udder support 106 Weak Strong
Udder depth 105 Deep High
Udder balance 115 Deep rear udder Deep front udder
Teat length 101 Short Long
Teat thickness 103 Thin Thick
Teat placement (front) 102 Wide Close
Teat placement (back) 115 Wide Close

NAV proof run date: 03-12-2024 Reliability 96 % Number of daughters: 2399

Monogenic

Name Scientific name Symptoms Code Result
BLAD Bovine Leukocyte Adhesion Deficiency (BLF = Not carrier, BLC = Single carrier, BLS = Double carrier) BLAD is an autosomal Read more (BLF = Not carrier, BLC = Single carrier, BLS = Double carrier) BLAD is an autosomal recessively inherited defect in the Holstein population. It is characterized by recurrent bacterial infections, delayed wound healing and stunted growth. Calves with BLAD are more susceptible to infections and their lifespan varies, many die shortly after birth. Osborndale Ivanhoe (US 1189870) has been identified as the key ancestor of the disorder. Several widely used sires after Osborndale, eg. Penstate Ivanhoe Star (US 1441440) and Carlin-M Ivanhoe Bell (US 1667366) are carriers of BLAD. https://omia.org/OMIA000595/9913/ BLF Free
HH1 Holstein Haplotype 1 (HH1F = Not carrier, HH1C = Single carrier, HH1S = Double carrier) HH1 is an autosomal Read more (HH1F = Not carrier, HH1C = Single carrier, HH1S = Double carrier) HH1 is an autosomal recessively inherited defect in the Holstein population. The disorder was identified in the North American Holstein population and primarily causes early embryonic death (spontaneous abortion), but abortion can occur throughout the gestation. The key ancestor is believed to be Pawnee Farm Arlinda Chief (US1427381). https://omia.org/OMIA000001/9913/ HH1F Free
HH3 Holstein Haplotype 3 (HH3F = Not carrier, HH3C = Single carrier, HH3S = Double carrier) HH3 is an autosomal Read more (HH3F = Not carrier, HH3C = Single carrier, HH3S = Double carrier) HH3 is an autosomal recessively inherited defect in the Holstein population. The disorder has been identified in the North American and the Nordic Holstein population, however the frequency was somewhat lower in the Nordic population. HH3 primarily causes early embryonic death (spontaneous abortion), within the first 60 days of gestation. The key ancestors are believed to be Glendell Arlinda Chief (US 1556373) and Gray View Skyliner (US 1244845). https://omia.org/OMIA001824/9913/ HH3F Free
HH4 Holstein Haplotype 4 (HH4F = Not carrier, HH4C = Single carrier, HH4S = Double carrier) HH4 is an autosomal Read more (HH4F = Not carrier, HH4C = Single carrier, HH4S = Double carrier) HH4 is an autosomal recessively inherited defect in the Holstein population. The disorder was identified in the French Holstein population and causes early embryonic death (spontaneous abortion). For animals that are a heterozygous for the gene, a reduction in fertility is seen. The effect is more pronounced in heifers than cows. The key ancestor is believed to be Besne Buck (FRA 4486041658). https://omia.org/OMIA001826/9913/ HH4F Free
RP1 Progressive retinal degeneration (RP1F = Not carrier, RP1C = Single carrier, RP1S = Double carrier) Progressive retinal degeneration is Read more (RP1F = Not carrier, RP1C = Single carrier, RP1S = Double carrier) Progressive retinal degeneration is an autosomal recessively inherited defect. In the French Normande population, an association between homozygotic carrier animals of the RP1 gene and progressive blindness has been demonstrated. Blindness is due to a progressive degeneration of the photoreceptors. The RP1 mutation segregates within many cattle populations and is prevalent in e.g. the Finncattle population. For other breeds than Normande the phenotypic effect of the mutation is unclear. https://omia.org/OMIA000866/9913/ RP1F Free
HH6 Holstein Haplotype 6 (HH6F = Not carrier, HH6C = Single carrier, HH6S = Double carrier) HH6 is an autosomal Read more (HH6F = Not carrier, HH6C = Single carrier, HH6S = Double carrier) HH6 is an autosomal recessively inherited defect in the Holstein population. It was identified in the French Holstein population and causes early embryonic death (spontaneous abortion), before 35 days of gestation. The key ancestor is believed to be Gray View Skyliner (US 1244845). https://omia.org/OMIA002149/9913/ HH6F Free
HH7 Holstein Haplotype 7 (HH7F = Not carrier, HH7C = Single carrier, HH7S = Double carrier) HH7 is an autosomal Read more (HH7F = Not carrier, HH7C = Single carrier, HH7S = Double carrier) HH7 is an autosomal recessively inherited defect in the Holstein population. It was identified in the French Holstein population and causes early embryonic death (spontaneous abortion), before 35 days of gestation. https://omia.org/OMIA001830/9913/ HH7F Free

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