VH Laust P - DNK 262806 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 120
Milk kg 101
Fat, kg 119
Fat, % 118
Protein kg 114
Protein % 122
Persistency 116
Growth 105
Daily carcass gain 92
Carcass conformation score 114
Saved feed 96
Maintenance efficiency 122

NAV proof run date: 06-05-2025 Reliability 87 % Number of daughters: 0

Expected Progeny Difference

Trait Index Bull effect Average
Milk lbs, 305 days 101 72.31 25,441.35
Fat lbs, 305 days 119 52.25 1,040.58
Fat %, 305 days 118 0.29 4.1
Protein lbs, 305 days 114 30.86 890.67
Protein %, 305 days 122 0.16 3.5

NAV proof run date: 06-05-2025 Reliability 87 % Number of daughters: 0

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 100
Interval from calving to first insemination (cows) 103
Interval from first to last insemination (heifers) 93
Interval from first to last insemination (cows) 106
Number of inseminations (heifers) 90
Number of inseminations (cows) 102
Calving sire 98
Calving maternal 102
Udder health 112
General health 111
Longevity 112
Hoof health 108
Sole Ulcer 107
Sole Hemorrhage 103
Heel Horn Erosion 106
Digital dermatitis + Interdigital Dermatitis 108
Verrucose dermatitis + Interdigital Hyperplasia 102
Double sole + White line separation 101
Cork screw claw 97
Youngstock survival 111

NAV proof run date: 06-05-2025 Reliability 80 % Number of daughters: 0

Functional

Trait Index 80 100 120
Milkability 95
Temperament 108

NAV proof run date: 06-05-2025 Reliability 63 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 81
Stature 77 Short Tall
Body depth 89 Shallow Deep
Chest width 98 Narrow Wide
Rib structure 92 Coarse Angular
Top line 98 Weak Strong
Rump width 88 Narrow pins Wide pins
Rump angle 100 High pins Low pins
Feet & legs 104
Rear legs, side view 89 Straight Sickled
Rear legs, back rear view 104 Toes out Parallel, bow-legged
Foot angle 100 Low Steep
Bone quality 106 Coarse Fine and thin
Hock quality 105 Filled Dry
Udder 107
Fore udder attachment 108 Loose Strong
Rear udder height 113 Low High
Rear udder width 109 Narrow Wide
Udder support 106 Weak Strong
Udder depth 96 Deep High
Udder balance 103 Deep rear udder Deep front udder
Teat length 106 Short Long
Teat thickness 116 Thin Thick
Teat placement (front) 94 Wide Close
Teat placement (back) 97 Wide Close

NAV proof run date: 06-05-2025 Reliability 63 % Number of daughters: 0

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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