VH Lilling - SWE 45142 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 111
Milk kg 97
Fat, kg 113
Fat, % 113
Protein kg 105
Protein % 113
Persistency 96
Growth 95
Daily carcass gain 105
Carcass conformation score 86
Saved feed 106
Maintenance efficiency 91

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 4509

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 97 -98.4 11702
Fat kg, 305 days 113 16.2 483
Fat %, 305 days 113 0.21 4.2
Protein kg, 305 days 105 5.0 413
Protein %, 305 days 113 0.09 3.5

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 4509

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 105
Interval from calving to first insemination (cows) 106
Interval from first to last insemination (heifers) 108
Interval from first to last insemination (cows) 105
Number of inseminations (heifers) 108
Number of inseminations (cows) 101
Calving sire 101
Calving maternal 97
Udder health 95
General health 111
Longevity 109
Hoof health 111
Sole Ulcer 107
Sole Hemorrhage 102
Heel Horn Erosion 108
Digital dermatitis + Interdigital Dermatitis 108
Verrucose dermatitis + Interdigital Hyperplasia 115
Double sole + White line separation 104
Cork screw claw 97
Youngstock survival 106

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 4457

Functional

Trait Index 80 100 120
Milkability 95
Temperament 112

NAV proof run date: 03-02-2026 Reliability 97 % Number of daughters: 1780

Conformation

Trait Index 80 100 120
Frame 110
Stature 105 Short Tall
Body depth 99 Shallow Deep
Chest width 106 Narrow Wide
Rib structure 105 Coarse Angular
Top line 90 Weak Strong
Rump width 119 Narrow pins Wide pins
Rump angle 103 High pins Low pins
Feet & legs 102
Rear legs, side view 107 Straight Sickled
Rear legs, back rear view 103 Toes out Parallel, bow-legged
Foot angle 103 Low Steep
Bone quality 101 Coarse Fine and thin
Hock quality 96 Filled Dry
Udder 113
Fore udder attachment 102 Loose Strong
Rear udder height 111 Low High
Rear udder width 113 Narrow Wide
Udder support 97 Weak Strong
Udder depth 114 Deep High
Udder balance 99 Deep rear udder Deep front udder
Teat length 109 Short Long
Teat thickness 100 Thin Thick
Teat placement (front) 98 Wide Close
Teat placement (back) 98 Wide Close

NAV proof run date: 03-02-2026 Reliability 97 % Number of daughters: 1780

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

Want to know more?
Send us a message.

Name

Country

Phone

Post code

Your message