VH NiraPRC - DNK 262186 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 106
Milk kg 87
Fat, kg 102
Fat, % 114
Protein kg 102
Protein % 126
Persistency 117
Growth 88
Daily carcass gain 92
Carcass conformation score 86
Saved feed 106
Maintenance efficiency 110

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 1773

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 87 -426.5 11758
Fat kg, 305 days 102 2.5 487
Fat %, 305 days 114 0.22 4.2
Protein kg, 305 days 102 2.0 416
Protein %, 305 days 126 0.19 3.6

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 1773

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 121
Interval from calving to first insemination (cows) 113
Interval from first to last insemination (heifers) 102
Interval from first to last insemination (cows) 123
Number of inseminations (heifers) 95
Number of inseminations (cows) 115
Calving sire 102
Calving maternal 105
Udder health 107
General health 106
Longevity 114
Hoof health 108
Sole Ulcer 103
Sole Hemorrhage 106
Heel Horn Erosion 106
Digital dermatitis + Interdigital Dermatitis 117
Verrucose dermatitis + Interdigital Hyperplasia 105
Double sole + White line separation 104
Cork screw claw 97
Youngstock survival 112

NAV proof run date: 05-05-2026 Reliability 97 % Number of daughters: 1460

Functional

Trait Index 80 100 120
Milkability 85
Temperament 110

NAV proof run date: 05-05-2026 Reliability 90 % Number of daughters: 283

Conformation

Trait Index 80 100 120
Frame 86
Stature 90 Short Tall
Body depth 87 Shallow Deep
Chest width 91 Narrow Wide
Rib structure 94 Coarse Angular
Top line 83 Weak Strong
Rump width 95 Narrow pins Wide pins
Rump angle 81 High pins Low pins
Feet & legs 107
Rear legs, side view 83 Straight Sickled
Rear legs, back rear view 97 Toes out Parallel, bow-legged
Foot angle 113 Low Steep
Bone quality 119 Coarse Fine and thin
Hock quality 105 Filled Dry
Udder 111
Fore udder attachment 117 Loose Strong
Rear udder height 96 Low High
Rear udder width 93 Narrow Wide
Udder support 95 Weak Strong
Udder depth 116 Deep High
Udder balance 113 Deep rear udder Deep front udder
Teat length 115 Short Long
Teat thickness 107 Thin Thick
Teat placement (front) 100 Wide Close
Teat placement (back) 104 Wide Close

NAV proof run date: 05-05-2026 Reliability 90 % Number of daughters: 283

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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