VH Namur P - DNK 261915 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 108
Milk kg 87
Fat, kg 106
Fat, % 116
Protein kg 102
Protein % 126
Persistency 101
Growth 116
Daily carcass gain 123
Carcass conformation score 105
Saved feed 103
Maintenance efficiency 92

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 1786

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 87 -426.5 11758
Fat kg, 305 days 106 7.5 487
Fat %, 305 days 116 0.26 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: 1786

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 104
Interval from calving to first insemination (cows) 107
Interval from first to last insemination (heifers) 92
Interval from first to last insemination (cows) 105
Number of inseminations (heifers) 97
Number of inseminations (cows) 103
Calving sire 99
Calving maternal 100
Udder health 101
General health 106
Longevity 104
Hoof health 91
Sole Ulcer 104
Sole Hemorrhage 92
Heel Horn Erosion 97
Digital dermatitis + Interdigital Dermatitis 64
Verrucose dermatitis + Interdigital Hyperplasia 81
Double sole + White line separation 95
Cork screw claw 108
Youngstock survival 100

NAV proof run date: 05-05-2026 Reliability 97 % Number of daughters: 1545

Functional

Trait Index 80 100 120
Milkability 85
Temperament 96

NAV proof run date: 05-05-2026 Reliability 92 % Number of daughters: 479

Conformation

Trait Index 80 100 120
Frame 106
Stature 104 Short Tall
Body depth 102 Shallow Deep
Chest width 110 Narrow Wide
Rib structure 99 Coarse Angular
Top line 95 Weak Strong
Rump width 103 Narrow pins Wide pins
Rump angle 104 High pins Low pins
Feet & legs 106
Rear legs, side view 103 Straight Sickled
Rear legs, back rear view 107 Toes out Parallel, bow-legged
Foot angle 96 Low Steep
Bone quality 99 Coarse Fine and thin
Hock quality 109 Filled Dry
Udder 103
Fore udder attachment 109 Loose Strong
Rear udder height 104 Low High
Rear udder width 101 Narrow Wide
Udder support 108 Weak Strong
Udder depth 113 Deep High
Udder balance 113 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) 112 Wide Close

NAV proof run date: 05-05-2026 Reliability 92 % Number of daughters: 479

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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