VH Laurids - DNK 261316 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 108
Milk kg 105
Fat, kg 102
Fat, % 97
Protein kg 112
Protein % 107
Persistency 108
Growth 80
Daily carcass gain 80
Carcass conformation score 85
Saved feed 113
Maintenance efficiency 110

NAV proof run date: 12-08-2025 Reliability 100 % Number of daughters: 3036

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 105 164.0 11600
Fat kg, 305 days 102 2.5 475
Fat %, 305 days 97 -0.05 4.1
Protein kg, 305 days 112 12.0 406
Protein %, 305 days 107 0.05 3.5

NAV proof run date: 12-08-2025 Reliability 100 % Number of daughters: 3036

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 113
Interval from calving to first insemination (cows) 94
Interval from first to last insemination (heifers) 113
Interval from first to last insemination (cows) 114
Number of inseminations (heifers) 113
Number of inseminations (cows) 114
Calving sire 104
Calving maternal 99
Udder health 102
General health 101
Longevity 106
Hoof health 94
Sole Ulcer 96
Sole Hemorrhage 77
Heel Horn Erosion 96
Digital dermatitis + Interdigital Dermatitis 109
Verrucose dermatitis + Interdigital Hyperplasia 93
Double sole + White line separation 92
Cork screw claw 80
Youngstock survival 109

NAV proof run date: 12-08-2025 Reliability 98 % Number of daughters: 2368

Functional

Trait Index 80 100 120
Milkability 93
Temperament 107

NAV proof run date: 12-08-2025 Reliability 93 % Number of daughters: 1085

Conformation

Trait Index 80 100 120
Frame 99
Stature 105 Short Tall
Body depth 98 Shallow Deep
Chest width 95 Narrow Wide
Rib structure 99 Coarse Angular
Top line 105 Weak Strong
Rump width 95 Narrow pins Wide pins
Rump angle 110 High pins Low pins
Feet & legs 96
Rear legs, side view 101 Straight Sickled
Rear legs, back rear view 88 Toes out Parallel, bow-legged
Foot angle 90 Low Steep
Bone quality 101 Coarse Fine and thin
Hock quality 111 Filled Dry
Udder 111
Fore udder attachment 110 Loose Strong
Rear udder height 103 Low High
Rear udder width 95 Narrow Wide
Udder support 104 Weak Strong
Udder depth 107 Deep High
Udder balance 90 Deep rear udder Deep front udder
Teat length 112 Short Long
Teat thickness 110 Thin Thick
Teat placement (front) 102 Wide Close
Teat placement (back) 104 Wide Close

NAV proof run date: 12-08-2025 Reliability 93 % Number of daughters: 1085

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

Want to know more?
Send us a message.

Name

Country

Phone

Post code

Your message