VH Finish - DNK 260952 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 113
Milk kg 122
Fat, kg 111
Fat, % 91
Protein kg 118
Protein % 90
Persistency 106
Growth 92
Daily carcass gain 99
Carcass conformation score 87
Saved feed 113
Maintenance efficiency 102

NAV proof run date: 02-09-2025 Reliability 100 % Number of daughters: 4453

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 122 721.8 11600
Fat kg, 305 days 111 13.7 475
Fat %, 305 days 91 -0.14 4.1
Protein kg, 305 days 118 18.0 406
Protein %, 305 days 90 -0.07 3.5

NAV proof run date: 02-09-2025 Reliability 100 % Number of daughters: 4453

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 110
Interval from calving to first insemination (cows) 96
Interval from first to last insemination (heifers) 116
Interval from first to last insemination (cows) 111
Number of inseminations (heifers) 110
Number of inseminations (cows) 107
Calving sire 99
Calving maternal 107
Udder health 90
General health 93
Longevity 107
Hoof health 104
Sole Ulcer 96
Sole Hemorrhage 91
Heel Horn Erosion 113
Digital dermatitis + Interdigital Dermatitis 118
Verrucose dermatitis + Interdigital Hyperplasia 109
Double sole + White line separation 98
Cork screw claw 91
Youngstock survival 106

NAV proof run date: 02-09-2025 Reliability 99 % Number of daughters: 4244

Functional

Trait Index 80 100 120
Milkability 115
Temperament 94

NAV proof run date: 02-09-2025 Reliability 96 % Number of daughters: 1878

Conformation

Trait Index 80 100 120
Frame 104
Stature 105 Short Tall
Body depth 100 Shallow Deep
Chest width 100 Narrow Wide
Rib structure 112 Coarse Angular
Top line 106 Weak Strong
Rump width 96 Narrow pins Wide pins
Rump angle 106 High pins Low pins
Feet & legs 106
Rear legs, side view 105 Straight Sickled
Rear legs, back rear view 100 Toes out Parallel, bow-legged
Foot angle 96 Low Steep
Bone quality 109 Coarse Fine and thin
Hock quality 107 Filled Dry
Udder 109
Fore udder attachment 109 Loose Strong
Rear udder height 131 Low High
Rear udder width 124 Narrow Wide
Udder support 97 Weak Strong
Udder depth 116 Deep High
Udder balance 110 Deep rear udder Deep front udder
Teat length 84 Short Long
Teat thickness 85 Thin Thick
Teat placement (front) 100 Wide Close
Teat placement (back) 105 Wide Close

NAV proof run date: 02-09-2025 Reliability 96 % Number of daughters: 1878

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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