VH Larsson - SWE 45168 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 119
Milk kg 108
Fat, kg 118
Fat, % 108
Protein kg 116
Protein % 109
Persistency 104
Growth 99
Daily carcass gain 83
Carcass conformation score 113
Saved feed 108
Maintenance efficiency 114

NAV proof run date: 03-11-2026 Reliability 99 % Number of daughters: 621

Expected Progeny Difference

Trait Index Bull effect Average
Milk lbs, 305 days 108 578.71 25,921.95
Fat lbs, 305 days 118 49.60 1,073.65
Fat %, 305 days 108 0.13 4.2
Protein lbs, 305 days 116 35.27 917.12
Protein %, 305 days 109 0.07 3.6

NAV proof run date: 03-11-2026 Reliability 99 % Number of daughters: 621

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 100
Interval from calving to first insemination (cows) 106
Interval from first to last insemination (heifers) 92
Interval from first to last insemination (cows) 102
Number of inseminations (heifers) 79
Number of inseminations (cows) 94
Calving sire 94
Calving maternal 99
Udder health 98
General health 106
Longevity 116
Hoof health 108
Sole Ulcer 100
Sole Hemorrhage 85
Heel Horn Erosion 114
Digital dermatitis + Interdigital Dermatitis 132
Verrucose dermatitis + Interdigital Hyperplasia 107
Double sole + White line separation 91
Cork screw claw 74
Youngstock survival 103

NAV proof run date: 03-11-2026 Reliability 96 % Number of daughters: 434

Functional

Trait Index 80 100 120
Milkability 96
Temperament 95

NAV proof run date: 03-11-2026 Reliability 88 % Number of daughters: 202

Conformation

Trait Index 80 100 120
Frame 80
Stature 75 Short Tall
Body depth 91 Shallow Deep
Chest width 96 Narrow Wide
Rib structure 94 Coarse Angular
Top line 95 Weak Strong
Rump width 86 Narrow pins Wide pins
Rump angle 87 High pins Low pins
Feet & legs 98
Rear legs, side view 87 Straight Sickled
Rear legs, back rear view 99 Toes out Parallel, bow-legged
Foot angle 103 Low Steep
Bone quality 104 Coarse Fine and thin
Hock quality 95 Filled Dry
Udder 101
Fore udder attachment 108 Loose Strong
Rear udder height 113 Low High
Rear udder width 113 Narrow Wide
Udder support 98 Weak Strong
Udder depth 89 Deep High
Udder balance 98 Deep rear udder Deep front udder
Teat length 95 Short Long
Teat thickness 112 Thin Thick
Teat placement (front) 98 Wide Close
Teat placement (back) 95 Wide Close

NAV proof run date: 03-11-2026 Reliability 88 % Number of daughters: 202

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