VH Solado - DNK 260791 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 105
Milk kg 93
Fat, kg 103
Fat, % 108
Protein kg 103
Protein % 116
Persistency 96
Growth 98
Daily carcass gain 106
Carcass conformation score 90
Saved feed 95
Maintenance efficiency 97

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 4498

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 93 -229.6 11600
Fat kg, 305 days 103 3.7 475
Fat %, 305 days 108 0.13 4.1
Protein kg, 305 days 103 3.0 406
Protein %, 305 days 116 0.12 3.5

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 4498

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 104
Calving sire 101
Calving maternal 105
Udder health 109
General health 107
Longevity 110
Hoof health 115
Sole Ulcer 108
Sole Hemorrhage 115
Heel Horn Erosion 116
Digital dermatitis + Interdigital Dermatitis 114
Verrucose dermatitis + Interdigital Hyperplasia 111
Double sole + White line separation 113
Cork screw claw 107
Youngstock survival 113

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 4480

Functional

Trait Index 80 100 120
Milkability 109
Temperament 94

NAV proof run date: 04-11-2025 Reliability 96 % Number of daughters: 1695

Conformation

Trait Index 80 100 120
Frame 99
Stature 98 Short Tall
Body depth 94 Shallow Deep
Chest width 102 Narrow Wide
Rib structure 102 Coarse Angular
Top line 80 Weak Strong
Rump width 103 Narrow pins Wide pins
Rump angle 82 High pins Low pins
Feet & legs 104
Rear legs, side view 109 Straight Sickled
Rear legs, back rear view 111 Toes out Parallel, bow-legged
Foot angle 100 Low Steep
Bone quality 96 Coarse Fine and thin
Hock quality 97 Filled Dry
Udder 120
Fore udder attachment 121 Loose Strong
Rear udder height 99 Low High
Rear udder width 105 Narrow Wide
Udder support 89 Weak Strong
Udder depth 117 Deep High
Udder balance 98 Deep rear udder Deep front udder
Teat length 95 Short Long
Teat thickness 100 Thin Thick
Teat placement (front) 106 Wide Close
Teat placement (back) 88 Wide Close

NAV proof run date: 04-11-2025 Reliability 96 % Number of daughters: 1695

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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