VH SummitP - DNK 263977 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 119
Milk kg 102
Fat, kg 125
Fat, % 119
Protein kg 108
Protein % 109
Persistency 117
Growth 100
Daily carcass gain 101
Carcass conformation score 99
Saved feed 112
Maintenance efficiency 106

NAV proof run date: 02-06-2026 Reliability 87 % Number of daughters: 0

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 102 65.6 11758
Fat kg, 305 days 125 31.2 487
Fat %, 305 days 119 0.30 4.2
Protein kg, 305 days 108 8.0 416
Protein %, 305 days 109 0.07 3.6

NAV proof run date: 02-06-2026 Reliability 87 % Number of daughters: 0

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 122
Interval from calving to first insemination (cows) 106
Interval from first to last insemination (heifers) 103
Interval from first to last insemination (cows) 124
Number of inseminations (heifers) 103
Number of inseminations (cows) 121
Calving sire 99
Calving maternal 105
Udder health 109
General health 109
Longevity 107
Hoof health 102
Sole Ulcer 102
Sole Hemorrhage 93
Heel Horn Erosion 97
Digital dermatitis + Interdigital Dermatitis 116
Verrucose dermatitis + Interdigital Hyperplasia 93
Double sole + White line separation 103
Cork screw claw 87
Youngstock survival 110

NAV proof run date: 02-06-2026 Reliability 77 % Number of daughters: 0

Functional

Trait Index 80 100 120
Milkability 104
Temperament 112

NAV proof run date: 02-06-2026 Reliability 58 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 95
Stature 98 Short Tall
Body depth 98 Shallow Deep
Chest width 94 Narrow Wide
Rib structure 100 Coarse Angular
Top line 99 Weak Strong
Rump width 94 Narrow pins Wide pins
Rump angle 97 High pins Low pins
Feet & legs 105
Rear legs, side view 108 Straight Sickled
Rear legs, back rear view 105 Toes out Parallel, bow-legged
Foot angle 94 Low Steep
Bone quality 108 Coarse Fine and thin
Hock quality 101 Filled Dry
Udder 104
Fore udder attachment 103 Loose Strong
Rear udder height 102 Low High
Rear udder width 104 Narrow Wide
Udder support 91 Weak Strong
Udder depth 104 Deep High
Udder balance 108 Deep rear udder Deep front udder
Teat length 115 Short Long
Teat thickness 108 Thin Thick
Teat placement (front) 88 Wide Close
Teat placement (back) 94 Wide Close

NAV proof run date: 02-06-2026 Reliability 58 % Number of daughters: 0

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