VH Reflux - DNK 262948 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 111
Milk kg 97
Fat, kg 119
Fat, % 118
Protein kg 99
Protein % 103
Persistency 113
Growth 104
Daily carcass gain 99
Carcass conformation score 106
Saved feed 100
Maintenance efficiency 115

NAV proof run date: 03-03-2026 Reliability 90 % Number of daughters: 0

Expected Progeny Difference

Trait Index Bull effect Average
Milk lbs, 305 days 97 -216.93 25,798.49
Fat lbs, 305 days 119 52.25 1,064.83
Fat %, 305 days 118 0.29 4.2
Protein lbs, 305 days 99 -2.20 910.51
Protein %, 305 days 103 0.02 3.5

NAV proof run date: 03-03-2026 Reliability 90 % Number of daughters: 0

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 115
Interval from calving to first insemination (cows) 111
Interval from first to last insemination (heifers) 94
Interval from first to last insemination (cows) 119
Number of inseminations (heifers) 91
Number of inseminations (cows) 108
Calving sire 104
Calving maternal 107
Udder health 110
General health 120
Longevity 122
Hoof health 114
Sole Ulcer 104
Sole Hemorrhage 108
Heel Horn Erosion 117
Digital dermatitis + Interdigital Dermatitis 121
Verrucose dermatitis + Interdigital Hyperplasia 117
Double sole + White line separation 104
Cork screw claw 115
Youngstock survival 117

NAV proof run date: 03-03-2026 Reliability 81 % Number of daughters: 0

Functional

Trait Index 80 100 120
Milkability 113
Temperament 114

NAV proof run date: 03-03-2026 Reliability 66 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 93
Stature 90 Short Tall
Body depth 89 Shallow Deep
Chest width 93 Narrow Wide
Rib structure 102 Coarse Angular
Top line 109 Weak Strong
Rump width 109 Narrow pins Wide pins
Rump angle 114 High pins Low pins
Feet & legs 100
Rear legs, side view 93 Straight Sickled
Rear legs, back rear view 98 Toes out Parallel, bow-legged
Foot angle 96 Low Steep
Bone quality 104 Coarse Fine and thin
Hock quality 106 Filled Dry
Udder 111
Fore udder attachment 114 Loose Strong
Rear udder height 104 Low High
Rear udder width 109 Narrow Wide
Udder support 83 Weak Strong
Udder depth 111 Deep High
Udder balance 88 Deep rear udder Deep front udder
Teat length 92 Short Long
Teat thickness 86 Thin Thick
Teat placement (front) 103 Wide Close
Teat placement (back) 89 Wide Close

NAV proof run date: 03-03-2026 Reliability 66 % 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