VH Laurids - I00914438 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 103
Milk kg 103
Fat, kg 97
Fat, % 95
Protein kg 108
Protein % 106
Persistency 108
Growth 80
Daily carcass gain 80
Carcass conformation score 86
Saved feed 112
Maintenance efficiency 113

NAV proof run date: 01-09-2026 Reliability 99 % Number of daughters: 3734

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 103 98.4 11758
Fat kg, 305 days 97 -3.7 487
Fat %, 305 days 95 -0.08 4.2
Protein kg, 305 days 108 8.0 416
Protein %, 305 days 106 0.04 3.6

NAV proof run date: 01-09-2026 Reliability 99 % Number of daughters: 3734

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 115
Interval from calving to first insemination (cows) 94
Interval from first to last insemination (heifers) 109
Interval from first to last insemination (cows) 116
Number of inseminations (heifers) 111
Number of inseminations (cows) 118
Calving sire 104
Calving maternal 98
Udder health 101
General health 99
Longevity 107
Hoof health 94
Sole Ulcer 97
Sole Hemorrhage 78
Heel Horn Erosion 97
Digital dermatitis + Interdigital Dermatitis 102
Verrucose dermatitis + Interdigital Hyperplasia 92
Double sole + White line separation 91
Cork screw claw 80
Youngstock survival 109

NAV proof run date: 01-09-2026 Reliability 99 % Number of daughters: 3136

Functional

Trait Index 80 100 120
Milkability 92
Temperament 111

NAV proof run date: 01-09-2026 Reliability 96 % Number of daughters: 1522

Conformation

Trait Index 80 100 120
Frame 98
Stature 104 Short Tall
Body depth 101 Shallow Deep
Chest width 93 Narrow Wide
Rib structure 100 Coarse Angular
Top line 106 Weak Strong
Rump width 94 Narrow pins Wide pins
Rump angle 110 High pins Low pins
Feet & legs 95
Rear legs, side view 104 Straight Sickled
Rear legs, back rear view 88 Toes out Parallel, bow-legged
Foot angle 88 Low Steep
Bone quality 103 Coarse Fine and thin
Hock quality 109 Filled Dry
Udder 110
Fore udder attachment 109 Loose Strong
Rear udder height 101 Low High
Rear udder width 99 Narrow Wide
Udder support 102 Weak Strong
Udder depth 105 Deep High
Udder balance 88 Deep rear udder Deep front udder
Teat length 112 Short Long
Teat thickness 110 Thin Thick
Teat placement (front) 101 Wide Close
Teat placement (back) 101 Wide Close

NAV proof run date: 01-09-2026 Reliability 96 % Number of daughters: 1522

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