VH Seo PRC - DEU 99542 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 107
Milk kg 96
Fat, kg 107
Fat, % 110
Protein kg 103
Protein % 111
Persistency 103
Growth 80
Daily carcass gain 85
Carcass conformation score 80
Saved feed 89
Maintenance efficiency 98

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 6786

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 96 -131.2 11600
Fat kg, 305 days 107 8.7 475
Fat %, 305 days 110 0.16 4.1
Protein kg, 305 days 103 3.0 406
Protein %, 305 days 111 0.08 3.5

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 6786

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 109
Calving sire 107
Calving maternal 98
Udder health 95
General health 101
Longevity 93
Hoof health 120
Sole Ulcer 108
Sole Hemorrhage 118
Heel Horn Erosion 121
Digital dermatitis + Interdigital Dermatitis 124
Verrucose dermatitis + Interdigital Hyperplasia 115
Double sole + White line separation 117
Cork screw claw 122
Youngstock survival 81

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 6380

Functional

Trait Index 80 100 120
Milkability 96
Temperament 101

NAV proof run date: 04-11-2025 Reliability 95 % Number of daughters: 2226

Conformation

Trait Index 80 100 120
Frame 102
Stature 114 Short Tall
Body depth 91 Shallow Deep
Chest width 89 Narrow Wide
Rib structure 109 Coarse Angular
Top line 104 Weak Strong
Rump width 101 Narrow pins Wide pins
Rump angle 95 High pins Low pins
Feet & legs 106
Rear legs, side view 100 Straight Sickled
Rear legs, back rear view 99 Toes out Parallel, bow-legged
Foot angle 108 Low Steep
Bone quality 110 Coarse Fine and thin
Hock quality 100 Filled Dry
Udder 120
Fore udder attachment 121 Loose Strong
Rear udder height 110 Low High
Rear udder width 104 Narrow Wide
Udder support 96 Weak Strong
Udder depth 126 Deep High
Udder balance 97 Deep rear udder Deep front udder
Teat length 105 Short Long
Teat thickness 95 Thin Thick
Teat placement (front) 112 Wide Close
Teat placement (back) 108 Wide Close

NAV proof run date: 04-11-2025 Reliability 95 % Number of daughters: 2226

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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