VH Mint PP - DNK 260636 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 105
Milk kg 100
Fat, kg 107
Fat, % 106
Protein kg 101
Protein % 102
Persistency 111
Growth 97
Daily carcass gain 102
Carcass conformation score 92
Saved feed 109
Maintenance efficiency 103

NAV proof run date: 06-05-2025 Reliability 99 % Number of daughters: 1118

Expected Progeny Difference

Trait Index Bull effect Average
Milk lbs, 305 days 100 0.00 25,441.35
Fat lbs, 305 days 107 19.18 1,040.58
Fat %, 305 days 106 0.10 4.1
Protein lbs, 305 days 101 2.20 890.67
Protein %, 305 days 102 0.01 3.5

NAV proof run date: 06-05-2025 Reliability 99 % Number of daughters: 1118

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 91
Interval from calving to first insemination (cows) 103
Interval from first to last insemination (heifers) 76
Interval from first to last insemination (cows) 97
Number of inseminations (heifers) 77
Number of inseminations (cows) 92
Calving sire 95
Calving maternal 87
Udder health 97
General health 108
Longevity 105
Hoof health 95
Sole Ulcer 103
Sole Hemorrhage 113
Heel Horn Erosion 87
Digital dermatitis + Interdigital Dermatitis 84
Verrucose dermatitis + Interdigital Hyperplasia 81
Double sole + White line separation 107
Cork screw claw 117
Youngstock survival 113

NAV proof run date: 06-05-2025 Reliability 98 % Number of daughters: 1152

Functional

Trait Index 80 100 120
Milkability 99
Temperament 116

NAV proof run date: 06-05-2025 Reliability 93 % Number of daughters: 452

Conformation

Trait Index 80 100 120
Frame 105
Stature 97 Short Tall
Body depth 107 Shallow Deep
Chest width 98 Narrow Wide
Rib structure 107 Coarse Angular
Top line 90 Weak Strong
Rump width 109 Narrow pins Wide pins
Rump angle 92 High pins Low pins
Feet & legs 108
Rear legs, side view 110 Straight Sickled
Rear legs, back rear view 117 Toes out Parallel, bow-legged
Foot angle 90 Low Steep
Bone quality 103 Coarse Fine and thin
Hock quality 103 Filled Dry
Udder 104
Fore udder attachment 109 Loose Strong
Rear udder height 106 Low High
Rear udder width 120 Narrow Wide
Udder support 106 Weak Strong
Udder depth 99 Deep High
Udder balance 116 Deep rear udder Deep front udder
Teat length 106 Short Long
Teat thickness 110 Thin Thick
Teat placement (front) 95 Wide Close
Teat placement (back) 103 Wide Close

NAV proof run date: 06-05-2025 Reliability 93 % Number of daughters: 452

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/ HH1C Carrier
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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