VH Nalegro - DNK 262385 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 119
Milk kg 104
Fat, kg 121
Fat, % 114
Protein kg 112
Protein % 110
Persistency 113
Growth 102
Daily carcass gain 96
Carcass conformation score 106
Saved feed 103
Maintenance efficiency 102

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 536

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 104 131.2 11702
Fat kg, 305 days 121 26.2 483
Fat %, 305 days 114 0.22 4.2
Protein kg, 305 days 112 12.0 413
Protein %, 305 days 110 0.07 3.5

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 536

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 108
Interval from calving to first insemination (cows) 108
Interval from first to last insemination (heifers) 94
Interval from first to last insemination (cows) 111
Number of inseminations (heifers) 90
Number of inseminations (cows) 102
Calving sire 103
Calving maternal 105
Udder health 101
General health 102
Longevity 108
Hoof health 108
Sole Ulcer 105
Sole Hemorrhage 107
Heel Horn Erosion 101
Digital dermatitis + Interdigital Dermatitis 107
Verrucose dermatitis + Interdigital Hyperplasia 113
Double sole + White line separation 103
Cork screw claw 104
Youngstock survival 73

NAV proof run date: 03-02-2026 Reliability 89 % Number of daughters: 329

Functional

Trait Index 80 100 120
Milkability 101
Temperament 88

NAV proof run date: 03-02-2026 Reliability 81 % Number of daughters: 47

Conformation

Trait Index 80 100 120
Frame 100
Stature 106 Short Tall
Body depth 97 Shallow Deep
Chest width 83 Narrow Wide
Rib structure 103 Coarse Angular
Top line 92 Weak Strong
Rump width 113 Narrow pins Wide pins
Rump angle 106 High pins Low pins
Feet & legs 102
Rear legs, side view 94 Straight Sickled
Rear legs, back rear view 95 Toes out Parallel, bow-legged
Foot angle 102 Low Steep
Bone quality 110 Coarse Fine and thin
Hock quality 106 Filled Dry
Udder 110
Fore udder attachment 107 Loose Strong
Rear udder height 113 Low High
Rear udder width 102 Narrow Wide
Udder support 106 Weak Strong
Udder depth 115 Deep High
Udder balance 111 Deep rear udder Deep front udder
Teat length 102 Short Long
Teat thickness 108 Thin Thick
Teat placement (front) 101 Wide Close
Teat placement (back) 106 Wide Close

NAV proof run date: 03-02-2026 Reliability 81 % Number of daughters: 47

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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