VH SismoPP - 528HO2634 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 112
Milk kg 106
Fat, kg 110
Fat, % 103
Protein kg 112
Protein % 107
Persistency 111
Growth 95
Daily carcass gain 105
Carcass conformation score 87
Saved feed 84
Maintenance efficiency 85

NAV proof run date: 03-03-2026 Reliability 91 % Number of daughters: 0

Expected Progeny Difference

Trait Index Bull effect Average
Milk lbs, 305 days 106 433.87 25,798.49
Fat lbs, 305 days 110 27.56 1,064.83
Fat %, 305 days 103 0.05 4.2
Protein lbs, 305 days 112 26.46 910.51
Protein %, 305 days 107 0.05 3.5

NAV proof run date: 03-03-2026 Reliability 91 % Number of daughters: 0

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 98
Interval from calving to first insemination (cows) 100
Interval from first to last insemination (heifers) 87
Interval from first to last insemination (cows) 101
Number of inseminations (heifers) 81
Number of inseminations (cows) 95
Calving sire 99
Calving maternal 106
Udder health 97
General health 104
Longevity 103
Hoof health 123
Sole Ulcer 116
Sole Hemorrhage 120
Heel Horn Erosion 110
Digital dermatitis + Interdigital Dermatitis 121
Verrucose dermatitis + Interdigital Hyperplasia 118
Double sole + White line separation 117
Cork screw claw 108
Youngstock survival 94

NAV proof run date: 03-03-2026 Reliability 82 % Number of daughters: 0

Functional

Trait Index 80 100 120
Milkability 106
Temperament 94

NAV proof run date: 03-03-2026 Reliability 68 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 119
Stature 121 Short Tall
Body depth 108 Shallow Deep
Chest width 112 Narrow Wide
Rib structure 104 Coarse Angular
Top line 111 Weak Strong
Rump width 108 Narrow pins Wide pins
Rump angle 109 High pins Low pins
Feet & legs 99
Rear legs, side view 92 Straight Sickled
Rear legs, back rear view 108 Toes out Parallel, bow-legged
Foot angle 119 Low Steep
Bone quality 81 Coarse Fine and thin
Hock quality 94 Filled Dry
Udder 116
Fore udder attachment 114 Loose Strong
Rear udder height 111 Low High
Rear udder width 107 Narrow Wide
Udder support 108 Weak Strong
Udder depth 106 Deep High
Udder balance 92 Deep rear udder Deep front udder
Teat length 116 Short Long
Teat thickness 109 Thin Thick
Teat placement (front) 99 Wide Close
Teat placement (back) 104 Wide Close

NAV proof run date: 03-03-2026 Reliability 68 % Number of daughters: 0

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