VH Bleech - DEU 362020433 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 116
Milk kg 94
Fat, kg 116
Fat, % 119
Protein kg 108
Protein % 121
Persistency 117
Growth 91
Daily carcass gain 104
Carcass conformation score 81
Saved feed 89
Maintenance efficiency 84

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 6673

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 94 -196.8 11600
Fat kg, 305 days 116 20.0 475
Fat %, 305 days 119 0.30 4.1
Protein kg, 305 days 108 8.0 406
Protein %, 305 days 121 0.15 3.5

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 6673

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 110
Calving sire 97
Calving maternal 100
Udder health 110
General health 111
Longevity 96
Hoof health 110
Sole Ulcer 102
Sole Hemorrhage 98
Heel Horn Erosion 115
Digital dermatitis + Interdigital Dermatitis 121
Verrucose dermatitis + Interdigital Hyperplasia 111
Double sole + White line separation 110
Cork screw claw 93
Youngstock survival 103

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 5917

Functional

Trait Index 80 100 120
Milkability 105
Temperament 89

NAV proof run date: 04-11-2025 Reliability 96 % Number of daughters: 2539

Conformation

Trait Index 80 100 120
Frame 118
Stature 120 Short Tall
Body depth 111 Shallow Deep
Chest width 107 Narrow Wide
Rib structure 110 Coarse Angular
Top line 101 Weak Strong
Rump width 106 Narrow pins Wide pins
Rump angle 111 High pins Low pins
Feet & legs 105
Rear legs, side view 105 Straight Sickled
Rear legs, back rear view 101 Toes out Parallel, bow-legged
Foot angle 105 Low Steep
Bone quality 97 Coarse Fine and thin
Hock quality 108 Filled Dry
Udder 106
Fore udder attachment 97 Loose Strong
Rear udder height 92 Low High
Rear udder width 91 Narrow Wide
Udder support 113 Weak Strong
Udder depth 109 Deep High
Udder balance 92 Deep rear udder Deep front udder
Teat length 99 Short Long
Teat thickness 82 Thin Thick
Teat placement (front) 108 Wide Close
Teat placement (back) 102 Wide Close

NAV proof run date: 04-11-2025 Reliability 96 % Number of daughters: 2539

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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