VH Harry P - DEU 361199175

Production & Efficiency

Trait Index 80 100 120
Production 107
Milk kg 93
Fat, kg 105
Fat, % 111
Protein kg 103
Protein % 117
Persistency 100
Growth 94
Daily carcass gain 97
Carcass conformation score 93
Saved feed 72
Maintenance efficiency 92
Metabolic efficiency 80

NAV proof run date: 02-07-2024 Reliability 99 % Number of daughters: 5172

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 93 -229.6 11437
Fat kg, 305 days 105 6.2 466
Fat %, 305 days 111 0.18 4.1
Protein kg, 305 days 103 3.0 399
Protein %, 305 days 117 0.12 3.5

NAV proof run date: 02-07-2024 Reliability 99 % Number of daughters: 5172

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 111
Interval from calving to first insemination (cows) 107
Interval from first to last insemination (heifers) 119
Interval from first to last insemination (cows) 108
Number of inseminations (heifers) 120
Number of inseminations (cows) 111
Calving sire 106
Calving maternal 99
Udder health 103
General health 102
Longevity 105
Hoof health 109
Sole Ulcer 107
Sole Hemorrhage 106
Heel Horn Erosion 97
Digital dermatitis + Interdigital Dermatitis 114
Verrucose dermatitis + Interdigital Hyperplasia 107
Double sole + White line separation 119
Cork screw claw 103
Youngstock survival 108

NAV proof run date: 02-07-2024 Reliability 99 % Number of daughters: 4847

Functional

Trait Index 80 100 120
Milkability 111
Temperament 104

NAV proof run date: 02-07-2024 Reliability 95 % Number of daughters: 1727

Conformation

Trait Index 80 100 120
Frame 103
Stature 102 Short Tall
Body depth 108 Shallow Deep
Chest width 99 Narrow Wide
Rib structure 100 Coarse Angular
Top line 88 Weak Strong
Rump width 102 Narrow pins Wide pins
Rump angle 94 High pins Low pins
Feet & legs 112
Rear legs, side view 89 Straight Sickled
Rear legs, back rear view 115 Toes out Parallel, bow-legged
Foot angle 91 Low Steep
Bone quality 104 Coarse Fine and thin
Hock quality 113 Filled Dry
Udder 97
Fore udder attachment 99 Loose Strong
Rear udder height 96 Low High
Rear udder width 96 Narrow Wide
Udder support 107 Weak Strong
Udder depth 106 Deep High
Udder balance 115 Deep rear udder Deep front udder
Teat length 100 Short Long
Teat thickness 99 Thin Thick
Teat placement (front) 101 Wide Close
Teat placement (back) 116 Wide Close

NAV proof run date: 02-07-2024 Reliability 95 % Number of daughters: 1727

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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