VH Namur P - DNK 261915 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 106
Milk kg 86
Fat, kg 103
Fat, % 116
Protein kg 100
Protein % 126
Persistency 101
Growth 116
Daily carcass gain 121
Carcass conformation score 105
Saved feed 103
Maintenance efficiency 92

NAV proof run date: 11-08-2026 Reliability 99 % Number of daughters: 2315

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 86 -459.3 11758
Fat kg, 305 days 103 3.7 487
Fat %, 305 days 116 0.26 4.2
Protein kg, 305 days 100 0.0 416
Protein %, 305 days 126 0.19 3.6

NAV proof run date: 11-08-2026 Reliability 99 % Number of daughters: 2315

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 102
Interval from calving to first insemination (cows) 107
Interval from first to last insemination (heifers) 92
Interval from first to last insemination (cows) 102
Number of inseminations (heifers) 96
Number of inseminations (cows) 100
Calving sire 99
Calving maternal 98
Udder health 99
General health 108
Longevity 104
Hoof health 88
Sole Ulcer 102
Sole Hemorrhage 92
Heel Horn Erosion 94
Digital dermatitis + Interdigital Dermatitis 62
Verrucose dermatitis + Interdigital Hyperplasia 77
Double sole + White line separation 95
Cork screw claw 111
Youngstock survival 101

NAV proof run date: 11-08-2026 Reliability 98 % Number of daughters: 2087

Functional

Trait Index 80 100 120
Milkability 86
Temperament 95

NAV proof run date: 11-08-2026 Reliability 92 % Number of daughters: 698

Conformation

Trait Index 80 100 120
Frame 107
Stature 106 Short Tall
Body depth 103 Shallow Deep
Chest width 112 Narrow Wide
Rib structure 99 Coarse Angular
Top line 95 Weak Strong
Rump width 103 Narrow pins Wide pins
Rump angle 103 High pins Low pins
Feet & legs 105
Rear legs, side view 104 Straight Sickled
Rear legs, back rear view 106 Toes out Parallel, bow-legged
Foot angle 95 Low Steep
Bone quality 98 Coarse Fine and thin
Hock quality 108 Filled Dry
Udder 104
Fore udder attachment 110 Loose Strong
Rear udder height 103 Low High
Rear udder width 100 Narrow Wide
Udder support 109 Weak Strong
Udder depth 113 Deep High
Udder balance 112 Deep rear udder Deep front udder
Teat length 91 Short Long
Teat thickness 90 Thin Thick
Teat placement (front) 115 Wide Close
Teat placement (back) 111 Wide Close

NAV proof run date: 11-08-2026 Reliability 92 % Number of daughters: 698

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