VH Baford - I00915330 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 102
Milk kg 91
Fat, kg 106
Fat, % 113
Protein kg 95
Protein % 108
Persistency 105
Growth 89
Daily carcass gain 81
Carcass conformation score 99
Saved feed 93
Maintenance efficiency 121

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 516

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 91 -295.3 11600
Fat kg, 305 days 106 7.5 475
Fat %, 305 days 113 0.21 4.1
Protein kg, 305 days 95 -5.0 406
Protein %, 305 days 108 0.06 3.5

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 516

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 117
Calving sire 110
Calving maternal 102
Udder health 103
General health 123
Longevity 116
Hoof health 114
Sole Ulcer 109
Sole Hemorrhage 100
Heel Horn Erosion 114
Digital dermatitis + Interdigital Dermatitis 121
Verrucose dermatitis + Interdigital Hyperplasia 106
Double sole + White line separation 110
Cork screw claw 88
Youngstock survival 100

NAV proof run date: 04-11-2025 Reliability 95 % Number of daughters: 460

Functional

Trait Index 80 100 120
Milkability 106
Temperament 99

NAV proof run date: 04-11-2025 Reliability 87 % Number of daughters: 183

Conformation

Trait Index 80 100 120
Frame 81
Stature 88 Short Tall
Body depth 81 Shallow Deep
Chest width 85 Narrow Wide
Rib structure 93 Coarse Angular
Top line 93 Weak Strong
Rump width 92 Narrow pins Wide pins
Rump angle 98 High pins Low pins
Feet & legs 116
Rear legs, side view 89 Straight Sickled
Rear legs, back rear view 111 Toes out Parallel, bow-legged
Foot angle 97 Low Steep
Bone quality 126 Coarse Fine and thin
Hock quality 113 Filled Dry
Udder 106
Fore udder attachment 106 Loose Strong
Rear udder height 111 Low High
Rear udder width 108 Narrow Wide
Udder support 93 Weak Strong
Udder depth 107 Deep High
Udder balance 113 Deep rear udder Deep front udder
Teat length 95 Short Long
Teat thickness 90 Thin Thick
Teat placement (front) 115 Wide Close
Teat placement (back) 88 Wide Close

NAV proof run date: 04-11-2025 Reliability 87 % Number of daughters: 183

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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