VH Nader - DNK 260958 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 111
Milk kg 95
Fat, kg 108
Fat, % 111
Protein kg 107
Protein % 117
Persistency 106
Growth 91
Daily carcass gain 98
Carcass conformation score 87
Saved feed 118
Maintenance efficiency 99

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 7943

Expected Progeny Difference

Trait Index Bull effect Average
Milk lbs, 305 days 95 -361.56 25,573.62
Fat lbs, 305 days 108 22.05 1,047.20
Fat %, 305 days 111 0.18 4.1
Protein lbs, 305 days 107 15.43 895.08
Protein %, 305 days 117 0.12 3.5

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 7943

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 106
Calving sire 108
Calving maternal 102
Udder health 106
General health 107
Longevity 104
Hoof health 108
Sole Ulcer 111
Sole Hemorrhage 104
Heel Horn Erosion 100
Digital dermatitis + Interdigital Dermatitis 95
Verrucose dermatitis + Interdigital Hyperplasia 107
Double sole + White line separation 112
Cork screw claw 105
Youngstock survival 103

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 7443

Functional

Trait Index 80 100 120
Milkability 95
Temperament 101

NAV proof run date: 04-11-2025 Reliability 97 % Number of daughters: 2929

Conformation

Trait Index 80 100 120
Frame 108
Stature 118 Short Tall
Body depth 99 Shallow Deep
Chest width 98 Narrow Wide
Rib structure 108 Coarse Angular
Top line 100 Weak Strong
Rump width 100 Narrow pins Wide pins
Rump angle 105 High pins Low pins
Feet & legs 105
Rear legs, side view 85 Straight Sickled
Rear legs, back rear view 104 Toes out Parallel, bow-legged
Foot angle 97 Low Steep
Bone quality 107 Coarse Fine and thin
Hock quality 111 Filled Dry
Udder 103
Fore udder attachment 107 Loose Strong
Rear udder height 109 Low High
Rear udder width 95 Narrow Wide
Udder support 114 Weak Strong
Udder depth 114 Deep High
Udder balance 87 Deep rear udder Deep front udder
Teat length 92 Short Long
Teat thickness 94 Thin Thick
Teat placement (front) 119 Wide Close
Teat placement (back) 123 Wide Close

NAV proof run date: 04-11-2025 Reliability 97 % Number of daughters: 2929

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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