VH Hambor - DNK 262718 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 120
Milk kg 105
Fat, kg 120
Fat, % 112
Protein kg 115
Protein % 113
Persistency 109
Growth 108
Daily carcass gain 105
Carcass conformation score 107
Saved feed 88
Maintenance efficiency 101

NAV proof run date: 03-02-2026 Reliability 90 % Number of daughters: 0

Expected Progeny Difference

Trait Index Bull effect Average
Milk lbs, 305 days 105 361.56 25,798.49
Fat lbs, 305 days 120 55.12 1,064.83
Fat %, 305 days 112 0.19 4.2
Protein lbs, 305 days 115 33.07 910.51
Protein %, 305 days 113 0.09 3.5

NAV proof run date: 03-02-2026 Reliability 90 % Number of daughters: 0

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 102
Interval from calving to first insemination (cows) 110
Interval from first to last insemination (heifers) 87
Interval from first to last insemination (cows) 104
Number of inseminations (heifers) 88
Number of inseminations (cows) 97
Calving sire 98
Calving maternal 106
Udder health 102
General health 109
Longevity 108
Hoof health 101
Sole Ulcer 97
Sole Hemorrhage 100
Heel Horn Erosion 103
Digital dermatitis + Interdigital Dermatitis 105
Verrucose dermatitis + Interdigital Hyperplasia 111
Double sole + White line separation 99
Cork screw claw 110
Youngstock survival 99

NAV proof run date: 03-02-2026 Reliability 82 % Number of daughters: 0

Functional

Trait Index 80 100 120
Milkability 113
Temperament 104

NAV proof run date: 03-02-2026 Reliability 67 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 93
Stature 101 Short Tall
Body depth 89 Shallow Deep
Chest width 93 Narrow Wide
Rib structure 103 Coarse Angular
Top line 107 Weak Strong
Rump width 89 Narrow pins Wide pins
Rump angle 93 High pins Low pins
Feet & legs 103
Rear legs, side view 109 Straight Sickled
Rear legs, back rear view 112 Toes out Parallel, bow-legged
Foot angle 104 Low Steep
Bone quality 95 Coarse Fine and thin
Hock quality 92 Filled Dry
Udder 111
Fore udder attachment 107 Loose Strong
Rear udder height 99 Low High
Rear udder width 97 Narrow Wide
Udder support 93 Weak Strong
Udder depth 112 Deep High
Udder balance 96 Deep rear udder Deep front udder
Teat length 101 Short Long
Teat thickness 100 Thin Thick
Teat placement (front) 110 Wide Close
Teat placement (back) 94 Wide Close

NAV proof run date: 03-02-2026 Reliability 67 % 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/ HH1C Carrier
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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