VH Alberta - CAN 12652589 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 108
Milk kg 111
Fat, kg 107
Fat, % 97
Protein kg 110
Protein % 97
Persistency 99
Growth 112
Daily carcass gain 118
Carcass conformation score 102
Saved feed 109
Maintenance efficiency 83

NAV proof run date: 01-07-2025 Reliability 100 % Number of daughters: 3232

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 111 360.9 11540
Fat kg, 305 days 107 8.7 472
Fat %, 305 days 97 -0.05 4.1
Protein kg, 305 days 110 10.0 404
Protein %, 305 days 97 -0.02 3.5

NAV proof run date: 01-07-2025 Reliability 100 % Number of daughters: 3232

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 102
Interval from calving to first insemination (cows) 94
Interval from first to last insemination (heifers) 95
Interval from first to last insemination (cows) 104
Number of inseminations (heifers) 98
Number of inseminations (cows) 110
Calving sire 103
Calving maternal 100
Udder health 92
General health 92
Longevity 101
Hoof health 110
Sole Ulcer 106
Sole Hemorrhage 111
Heel Horn Erosion 102
Digital dermatitis + Interdigital Dermatitis 114
Verrucose dermatitis + Interdigital Hyperplasia 107
Double sole + White line separation 121
Cork screw claw 100
Youngstock survival 96

NAV proof run date: 01-07-2025 Reliability 99 % Number of daughters: 3268

Functional

Trait Index 80 100 120
Milkability 122
Temperament 107

NAV proof run date: 01-07-2025 Reliability 97 % Number of daughters: 1343

Conformation

Trait Index 80 100 120
Frame 112
Stature 110 Short Tall
Body depth 101 Shallow Deep
Chest width 108 Narrow Wide
Rib structure 103 Coarse Angular
Top line 87 Weak Strong
Rump width 115 Narrow pins Wide pins
Rump angle 97 High pins Low pins
Feet & legs 93
Rear legs, side view 115 Straight Sickled
Rear legs, back rear view 86 Toes out Parallel, bow-legged
Foot angle 97 Low Steep
Bone quality 94 Coarse Fine and thin
Hock quality 108 Filled Dry
Udder 112
Fore udder attachment 113 Loose Strong
Rear udder height 110 Low High
Rear udder width 103 Narrow Wide
Udder support 113 Weak Strong
Udder depth 117 Deep High
Udder balance 99 Deep rear udder Deep front udder
Teat length 89 Short Long
Teat thickness 91 Thin Thick
Teat placement (front) 105 Wide Close
Teat placement (back) 114 Wide Close

NAV proof run date: 01-07-2025 Reliability 97 % Number of daughters: 1343

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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