VH Ascari - I00914430 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 109
Milk kg 105
Fat, kg 105
Fat, % 100
Protein kg 110
Protein % 106
Persistency 94
Growth 108
Daily carcass gain 106
Carcass conformation score 107
Saved feed 93
Maintenance efficiency 92

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 6235

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 105 164.0 11702
Fat kg, 305 days 105 6.2 483
Fat %, 305 days 100 0.00 4.2
Protein kg, 305 days 110 10.0 413
Protein %, 305 days 106 0.04 3.5

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 6235

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 116
Interval from calving to first insemination (cows) 110
Interval from first to last insemination (heifers) 111
Interval from first to last insemination (cows) 117
Number of inseminations (heifers) 105
Number of inseminations (cows) 111
Calving sire 105
Calving maternal 96
Udder health 96
General health 110
Longevity 103
Hoof health 107
Sole Ulcer 94
Sole Hemorrhage 90
Heel Horn Erosion 115
Digital dermatitis + Interdigital Dermatitis 136
Verrucose dermatitis + Interdigital Hyperplasia 113
Double sole + White line separation 94
Cork screw claw 77
Youngstock survival 109

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 5743

Functional

Trait Index 80 100 120
Milkability 104
Temperament 104

NAV proof run date: 03-02-2026 Reliability 96 % Number of daughters: 2126

Conformation

Trait Index 80 100 120
Frame 100
Stature 98 Short Tall
Body depth 97 Shallow Deep
Chest width 98 Narrow Wide
Rib structure 103 Coarse Angular
Top line 113 Weak Strong
Rump width 107 Narrow pins Wide pins
Rump angle 106 High pins Low pins
Feet & legs 90
Rear legs, side view 107 Straight Sickled
Rear legs, back rear view 73 Toes out Parallel, bow-legged
Foot angle 93 Low Steep
Bone quality 105 Coarse Fine and thin
Hock quality 106 Filled Dry
Udder 109
Fore udder attachment 114 Loose Strong
Rear udder height 104 Low High
Rear udder width 100 Narrow Wide
Udder support 112 Weak Strong
Udder depth 110 Deep High
Udder balance 102 Deep rear udder Deep front udder
Teat length 99 Short Long
Teat thickness 107 Thin Thick
Teat placement (front) 102 Wide Close
Teat placement (back) 114 Wide Close

NAV proof run date: 03-02-2026 Reliability 96 % Number of daughters: 2126

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/ HH4C Carrier
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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