VH Skills - DEU 362071912 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 128
Milk kg 129
Fat, kg 127
Fat, % 98
Protein kg 129
Protein % 95
Persistency 118
Growth 120
Daily carcass gain 114
Carcass conformation score 118
Saved feed 105
Maintenance efficiency 96

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 1075

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 129 951.4 11633
Fat kg, 305 days 127 33.7 477
Fat %, 305 days 98 -0.03 4.2
Protein kg, 305 days 129 29.0 409
Protein %, 305 days 95 -0.04 3.5

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 1075

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 109
Interval from calving to first insemination (cows) 103
Interval from first to last insemination (heifers) 115
Interval from first to last insemination (cows) 108
Number of inseminations (heifers) 116
Number of inseminations (cows) 105
Calving sire 102
Calving maternal 105
Udder health 100
General health 97
Longevity 117
Hoof health 104
Sole Ulcer 100
Sole Hemorrhage 100
Heel Horn Erosion 109
Digital dermatitis + Interdigital Dermatitis 107
Verrucose dermatitis + Interdigital Hyperplasia 104
Double sole + White line separation 103
Cork screw claw 101
Youngstock survival 105

NAV proof run date: 04-11-2025 Reliability 95 % Number of daughters: 805

Functional

Trait Index 80 100 120
Milkability 117
Temperament 112

NAV proof run date: 04-11-2025 Reliability 85 % Number of daughters: 312

Conformation

Trait Index 80 100 120
Frame 103
Stature 97 Short Tall
Body depth 99 Shallow Deep
Chest width 110 Narrow Wide
Rib structure 99 Coarse Angular
Top line 94 Weak Strong
Rump width 108 Narrow pins Wide pins
Rump angle 97 High pins Low pins
Feet & legs 84
Rear legs, side view 83 Straight Sickled
Rear legs, back rear view 84 Toes out Parallel, bow-legged
Foot angle 108 Low Steep
Bone quality 91 Coarse Fine and thin
Hock quality 89 Filled Dry
Udder 108
Fore udder attachment 118 Loose Strong
Rear udder height 104 Low High
Rear udder width 106 Narrow Wide
Udder support 104 Weak Strong
Udder depth 101 Deep High
Udder balance 101 Deep rear udder Deep front udder
Teat length 108 Short Long
Teat thickness 91 Thin Thick
Teat placement (front) 108 Wide Close
Teat placement (back) 105 Wide Close

NAV proof run date: 04-11-2025 Reliability 85 % Number of daughters: 312

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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