VH Bullboy - FIN 99010 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 94
Milk kg 96
Fat, kg 97
Fat, % 100
Protein kg 92
Protein % 94
Persistency 129
Growth 88
Daily carcass gain 85
Carcass conformation score 93
Saved feed 104
Maintenance efficiency 116

NAV proof run date: 02-09-2025 Reliability 100 % Number of daughters: 2910

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 96 -131.2 11600
Fat kg, 305 days 97 -3.7 475
Fat %, 305 days 100 0.00 4.1
Protein kg, 305 days 92 -8.0 406
Protein %, 305 days 94 -0.04 3.5

NAV proof run date: 02-09-2025 Reliability 100 % Number of daughters: 2910

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 116
Interval from calving to first insemination (cows) 107
Interval from first to last insemination (heifers) 110
Interval from first to last insemination (cows) 115
Number of inseminations (heifers) 107
Number of inseminations (cows) 117
Calving sire 101
Calving maternal 103
Udder health 98
General health 104
Longevity 100
Hoof health 114
Sole Ulcer 111
Sole Hemorrhage 100
Heel Horn Erosion 116
Digital dermatitis + Interdigital Dermatitis 108
Verrucose dermatitis + Interdigital Hyperplasia 108
Double sole + White line separation 111
Cork screw claw 88
Youngstock survival 98

NAV proof run date: 02-09-2025 Reliability 99 % Number of daughters: 3027

Functional

Trait Index 80 100 120
Milkability 127
Temperament 113

NAV proof run date: 02-09-2025 Reliability 97 % Number of daughters: 1315

Conformation

Trait Index 80 100 120
Frame 79
Stature 81 Short Tall
Body depth 89 Shallow Deep
Chest width 87 Narrow Wide
Rib structure 92 Coarse Angular
Top line 88 Weak Strong
Rump width 88 Narrow pins Wide pins
Rump angle 83 High pins Low pins
Feet & legs 107
Rear legs, side view 118 Straight Sickled
Rear legs, back rear view 99 Toes out Parallel, bow-legged
Foot angle 108 Low Steep
Bone quality 107 Coarse Fine and thin
Hock quality 109 Filled Dry
Udder 107
Fore udder attachment 109 Loose Strong
Rear udder height 88 Low High
Rear udder width 85 Narrow Wide
Udder support 89 Weak Strong
Udder depth 108 Deep High
Udder balance 97 Deep rear udder Deep front udder
Teat length 105 Short Long
Teat thickness 98 Thin Thick
Teat placement (front) 100 Wide Close
Teat placement (back) 85 Wide Close

NAV proof run date: 02-09-2025 Reliability 97 % Number of daughters: 1315

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/ HH3C Carrier
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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