VH SovranP - I00915322 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 116
Milk kg 114
Fat, kg 110
Fat, % 96
Protein kg 120
Protein % 106
Persistency 97
Growth 106
Daily carcass gain 117
Carcass conformation score 94
Saved feed 91
Maintenance efficiency 82

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 3733

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 114 459.3 11702
Fat kg, 305 days 110 12.5 483
Fat %, 305 days 96 -0.06 4.2
Protein kg, 305 days 120 20.0 413
Protein %, 305 days 106 0.04 3.5

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 3733

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 107
Interval from calving to first insemination (cows) 107
Interval from first to last insemination (heifers) 96
Interval from first to last insemination (cows) 110
Number of inseminations (heifers) 92
Number of inseminations (cows) 99
Calving sire 96
Calving maternal 107
Udder health 97
General health 104
Longevity 103
Hoof health 109
Sole Ulcer 106
Sole Hemorrhage 110
Heel Horn Erosion 102
Digital dermatitis + Interdigital Dermatitis 109
Verrucose dermatitis + Interdigital Hyperplasia 109
Double sole + White line separation 110
Cork screw claw 102
Youngstock survival 110

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 3442

Functional

Trait Index 80 100 120
Milkability 98
Temperament 98

NAV proof run date: 03-02-2026 Reliability 95 % Number of daughters: 1387

Conformation

Trait Index 80 100 120
Frame 128
Stature 122 Short Tall
Body depth 117 Shallow Deep
Chest width 116 Narrow Wide
Rib structure 115 Coarse Angular
Top line 95 Weak Strong
Rump width 116 Narrow pins Wide pins
Rump angle 95 High pins Low pins
Feet & legs 97
Rear legs, side view 108 Straight Sickled
Rear legs, back rear view 112 Toes out Parallel, bow-legged
Foot angle 112 Low Steep
Bone quality 74 Coarse Fine and thin
Hock quality 87 Filled Dry
Udder 110
Fore udder attachment 111 Loose Strong
Rear udder height 102 Low High
Rear udder width 110 Narrow Wide
Udder support 105 Weak Strong
Udder depth 107 Deep High
Udder balance 99 Deep rear udder Deep front udder
Teat length 123 Short Long
Teat thickness 120 Thin Thick
Teat placement (front) 100 Wide Close
Teat placement (back) 107 Wide Close

NAV proof run date: 03-02-2026 Reliability 95 % Number of daughters: 1387

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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