VH Yngvar - DEU 361229595 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 99
Milk kg 94
Fat, kg 104
Fat, % 108
Protein kg 93
Protein % 99
Persistency 104
Growth 98
Daily carcass gain 110
Carcass conformation score 87
Saved feed 103
Maintenance efficiency 93

NAV proof run date: 06-01-2026 Reliability 99 % Number of daughters: 5029

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 94 -196.8 11633
Fat kg, 305 days 104 5.0 477
Fat %, 305 days 108 0.13 4.2
Protein kg, 305 days 93 -7.0 409
Protein %, 305 days 99 -0.01 3.5

NAV proof run date: 06-01-2026 Reliability 99 % Number of daughters: 5029

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 100
Interval from calving to first insemination (cows) 86
Interval from first to last insemination (heifers) 97
Interval from first to last insemination (cows) 100
Number of inseminations (heifers) 100
Number of inseminations (cows) 110
Calving sire 104
Calving maternal 107
Udder health 107
General health 110
Longevity 104
Hoof health 102
Sole Ulcer 100
Sole Hemorrhage 101
Heel Horn Erosion 106
Digital dermatitis + Interdigital Dermatitis 92
Verrucose dermatitis + Interdigital Hyperplasia 109
Double sole + White line separation 106
Cork screw claw 105
Youngstock survival 91

NAV proof run date: 06-01-2026 Reliability 99 % Number of daughters: 4851

Functional

Trait Index 80 100 120
Milkability 100
Temperament 108

NAV proof run date: 06-01-2026 Reliability 95 % Number of daughters: 1689

Conformation

Trait Index 80 100 120
Frame 107
Stature 109 Short Tall
Body depth 98 Shallow Deep
Chest width 103 Narrow Wide
Rib structure 105 Coarse Angular
Top line 105 Weak Strong
Rump width 107 Narrow pins Wide pins
Rump angle 93 High pins Low pins
Feet & legs 108
Rear legs, side view 114 Straight Sickled
Rear legs, back rear view 102 Toes out Parallel, bow-legged
Foot angle 92 Low Steep
Bone quality 108 Coarse Fine and thin
Hock quality 117 Filled Dry
Udder 117
Fore udder attachment 124 Loose Strong
Rear udder height 117 Low High
Rear udder width 113 Narrow Wide
Udder support 108 Weak Strong
Udder depth 133 Deep High
Udder balance 116 Deep rear udder Deep front udder
Teat length 81 Short Long
Teat thickness 87 Thin Thick
Teat placement (front) 114 Wide Close
Teat placement (back) 120 Wide Close

NAV proof run date: 06-01-2026 Reliability 95 % Number of daughters: 1689

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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