VH Nalegro - DNK 262385 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 118
Milk kg 99
Fat, kg 122
Fat, % 119
Protein kg 109
Protein % 113
Persistency 115
Growth 101
Daily carcass gain 96
Carcass conformation score 106
Saved feed 95
Maintenance efficiency 103

NAV proof run date: 03-11-2026 Reliability 99 % Number of daughters: 3955

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 99 -32.8 11758
Fat kg, 305 days 122 27.5 487
Fat %, 305 days 119 0.30 4.2
Protein kg, 305 days 109 9.0 416
Protein %, 305 days 113 0.09 3.6

NAV proof run date: 03-11-2026 Reliability 99 % Number of daughters: 3955

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 107
Interval from calving to first insemination (cows) 108
Interval from first to last insemination (heifers) 95
Interval from first to last insemination (cows) 109
Number of inseminations (heifers) 90
Number of inseminations (cows) 100
Calving sire 103
Calving maternal 103
Udder health 101
General health 102
Longevity 107
Hoof health 102
Sole Ulcer 102
Sole Hemorrhage 105
Heel Horn Erosion 98
Digital dermatitis + Interdigital Dermatitis 105
Verrucose dermatitis + Interdigital Hyperplasia 99
Double sole + White line separation 99
Cork screw claw 102
Youngstock survival 76

NAV proof run date: 03-11-2026 Reliability 99 % Number of daughters: 3541

Functional

Trait Index 80 100 120
Milkability 107
Temperament 80

NAV proof run date: 03-11-2026 Reliability 91 % Number of daughters: 1138

Conformation

Trait Index 80 100 120
Frame 106
Stature 108 Short Tall
Body depth 98 Shallow Deep
Chest width 90 Narrow Wide
Rib structure 105 Coarse Angular
Top line 92 Weak Strong
Rump width 118 Narrow pins Wide pins
Rump angle 110 High pins Low pins
Feet & legs 99
Rear legs, side view 96 Straight Sickled
Rear legs, back rear view 94 Toes out Parallel, bow-legged
Foot angle 105 Low Steep
Bone quality 102 Coarse Fine and thin
Hock quality 100 Filled Dry
Udder 106
Fore udder attachment 104 Loose Strong
Rear udder height 113 Low High
Rear udder width 104 Narrow Wide
Udder support 106 Weak Strong
Udder depth 110 Deep High
Udder balance 113 Deep rear udder Deep front udder
Teat length 100 Short Long
Teat thickness 109 Thin Thick
Teat placement (front) 98 Wide Close
Teat placement (back) 106 Wide Close

NAV proof run date: 03-11-2026 Reliability 91 % Number of daughters: 1138

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