VH Nalegro - DNK 262385 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 117
Milk kg 98
Fat, kg 120
Fat, % 118
Protein kg 108
Protein % 115
Persistency 109
Growth 103
Daily carcass gain 97
Carcass conformation score 106
Saved feed 86
Maintenance efficiency 107

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 1675

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 98 -65.6 11758
Fat kg, 305 days 120 25.0 487
Fat %, 305 days 118 0.29 4.2
Protein kg, 305 days 108 8.0 416
Protein %, 305 days 115 0.11 3.6

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 1675

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 109
Interval from calving to first insemination (cows) 107
Interval from first to last insemination (heifers) 94
Interval from first to last insemination (cows) 112
Number of inseminations (heifers) 90
Number of inseminations (cows) 101
Calving sire 103
Calving maternal 106
Udder health 102
General health 99
Longevity 108
Hoof health 103
Sole Ulcer 103
Sole Hemorrhage 109
Heel Horn Erosion 96
Digital dermatitis + Interdigital Dermatitis 103
Verrucose dermatitis + Interdigital Hyperplasia 104
Double sole + White line separation 103
Cork screw claw 104
Youngstock survival 74

NAV proof run date: 05-05-2026 Reliability 97 % Number of daughters: 1333

Functional

Trait Index 80 100 120
Milkability 103
Temperament 80

NAV proof run date: 05-05-2026 Reliability 90 % Number of daughters: 323

Conformation

Trait Index 80 100 120
Frame 102
Stature 107 Short Tall
Body depth 96 Shallow Deep
Chest width 86 Narrow Wide
Rib structure 106 Coarse Angular
Top line 92 Weak Strong
Rump width 115 Narrow pins Wide pins
Rump angle 109 High pins Low pins
Feet & legs 98
Rear legs, side view 93 Straight Sickled
Rear legs, back rear view 93 Toes out Parallel, bow-legged
Foot angle 107 Low Steep
Bone quality 103 Coarse Fine and thin
Hock quality 99 Filled Dry
Udder 108
Fore udder attachment 106 Loose Strong
Rear udder height 114 Low High
Rear udder width 105 Narrow Wide
Udder support 109 Weak Strong
Udder depth 112 Deep High
Udder balance 114 Deep rear udder Deep front udder
Teat length 101 Short Long
Teat thickness 109 Thin Thick
Teat placement (front) 100 Wide Close
Teat placement (back) 107 Wide Close

NAV proof run date: 05-05-2026 Reliability 90 % Number of daughters: 323

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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