VH Lilling - SWE 45142 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 114
Milk kg 99
Fat, kg 115
Fat, % 114
Protein kg 108
Protein % 114
Persistency 100
Growth 95
Daily carcass gain 106
Carcass conformation score 85
Saved feed 106
Maintenance efficiency 88

NAV proof run date: 01-04-2025 Reliability 99 % Number of daughters: 4285

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 99 -32.8 11540
Fat kg, 305 days 115 18.7 472
Fat %, 305 days 114 0.22 4.1
Protein kg, 305 days 108 8.0 404
Protein %, 305 days 114 0.10 3.5

NAV proof run date: 01-04-2025 Reliability 99 % Number of daughters: 4285

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) 110
Interval from first to last insemination (cows) 106
Number of inseminations (heifers) 109
Number of inseminations (cows) 101
Calving sire 101
Calving maternal 98
Udder health 99
General health 113
Longevity 111
Hoof health 109
Sole Ulcer 104
Sole Hemorrhage 100
Heel Horn Erosion 108
Digital dermatitis + Interdigital Dermatitis 112
Verrucose dermatitis + Interdigital Hyperplasia 115
Double sole + White line separation 105
Cork screw claw 96
Youngstock survival 107

NAV proof run date: 01-04-2025 Reliability 99 % Number of daughters: 4295

Functional

Trait Index 80 100 120
Milkability 96
Temperament 111

NAV proof run date: 01-04-2025 Reliability 96 % Number of daughters: 1668

Conformation

Trait Index 80 100 120
Frame 112
Stature 106 Short Tall
Body depth 100 Shallow Deep
Chest width 108 Narrow Wide
Rib structure 105 Coarse Angular
Top line 90 Weak Strong
Rump width 121 Narrow pins Wide pins
Rump angle 102 High pins Low pins
Feet & legs 104
Rear legs, side view 108 Straight Sickled
Rear legs, back rear view 104 Toes out Parallel, bow-legged
Foot angle 106 Low Steep
Bone quality 100 Coarse Fine and thin
Hock quality 96 Filled Dry
Udder 113
Fore udder attachment 105 Loose Strong
Rear udder height 111 Low High
Rear udder width 115 Narrow Wide
Udder support 99 Weak Strong
Udder depth 114 Deep High
Udder balance 101 Deep rear udder Deep front udder
Teat length 110 Short Long
Teat thickness 99 Thin Thick
Teat placement (front) 98 Wide Close
Teat placement (back) 100 Wide Close

NAV proof run date: 01-04-2025 Reliability 96 % Number of daughters: 1668

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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