VH SovranP - DNK 261567 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 115
Milk kg 113
Fat, kg 108
Fat, % 95
Protein kg 119
Protein % 105
Persistency 97
Growth 105
Daily carcass gain 116
Carcass conformation score 94
Saved feed 98
Maintenance efficiency 84

NAV proof run date: 03-11-2026 Reliability 99 % Number of daughters: 3991

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 113 426.5 11758
Fat kg, 305 days 108 10.0 487
Fat %, 305 days 95 -0.08 4.2
Protein kg, 305 days 119 19.0 416
Protein %, 305 days 105 0.04 3.6

NAV proof run date: 03-11-2026 Reliability 99 % Number of daughters: 3991

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 104
Interval from calving to first insemination (cows) 105
Interval from first to last insemination (heifers) 96
Interval from first to last insemination (cows) 106
Number of inseminations (heifers) 92
Number of inseminations (cows) 97
Calving sire 96
Calving maternal 107
Udder health 96
General health 106
Longevity 110
Hoof health 110
Sole Ulcer 107
Sole Hemorrhage 111
Heel Horn Erosion 104
Digital dermatitis + Interdigital Dermatitis 109
Verrucose dermatitis + Interdigital Hyperplasia 107
Double sole + White line separation 113
Cork screw claw 103
Youngstock survival 111

NAV proof run date: 03-11-2026 Reliability 99 % Number of daughters: 3560

Functional

Trait Index 80 100 120
Milkability 98
Temperament 98

NAV proof run date: 03-11-2026 Reliability 95 % Number of daughters: 1515

Conformation

Trait Index 80 100 120
Frame 126
Stature 122 Short Tall
Body depth 116 Shallow Deep
Chest width 114 Narrow Wide
Rib structure 115 Coarse Angular
Top line 96 Weak Strong
Rump width 114 Narrow pins Wide pins
Rump angle 97 High pins Low pins
Feet & legs 96
Rear legs, side view 110 Straight Sickled
Rear legs, back rear view 111 Toes out Parallel, bow-legged
Foot angle 110 Low Steep
Bone quality 76 Coarse Fine and thin
Hock quality 88 Filled Dry
Udder 110
Fore udder attachment 109 Loose Strong
Rear udder height 101 Low High
Rear udder width 111 Narrow Wide
Udder support 106 Weak Strong
Udder depth 107 Deep High
Udder balance 97 Deep rear udder Deep front udder
Teat length 124 Short Long
Teat thickness 119 Thin Thick
Teat placement (front) 100 Wide Close
Teat placement (back) 106 Wide Close

NAV proof run date: 03-11-2026 Reliability 95 % Number of daughters: 1515

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