VH Putur - DNK 261904 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 117
Milk kg 99
Fat, kg 118
Fat, % 116
Protein kg 110
Protein % 116
Persistency 95
Growth 96
Daily carcass gain 101
Carcass conformation score 92
Saved feed 96
Maintenance efficiency 91

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 4499

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 99 -32.8 11758
Fat kg, 305 days 118 22.5 487
Fat %, 305 days 116 0.26 4.2
Protein kg, 305 days 110 10.0 416
Protein %, 305 days 116 0.12 3.6

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 4499

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 110
Interval from calving to first insemination (cows) 115
Interval from first to last insemination (heifers) 91
Interval from first to last insemination (cows) 111
Number of inseminations (heifers) 96
Number of inseminations (cows) 107
Calving sire 93
Calving maternal 96
Udder health 96
General health 107
Longevity 104
Hoof health 101
Sole Ulcer 99
Sole Hemorrhage 113
Heel Horn Erosion 99
Digital dermatitis + Interdigital Dermatitis 106
Verrucose dermatitis + Interdigital Hyperplasia 94
Double sole + White line separation 103
Cork screw claw 110
Youngstock survival 91

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 4005

Functional

Trait Index 80 100 120
Milkability 113
Temperament 107

NAV proof run date: 05-05-2026 Reliability 94 % Number of daughters: 1420

Conformation

Trait Index 80 100 120
Frame 116
Stature 110 Short Tall
Body depth 111 Shallow Deep
Chest width 103 Narrow Wide
Rib structure 115 Coarse Angular
Top line 110 Weak Strong
Rump width 112 Narrow pins Wide pins
Rump angle 110 High pins Low pins
Feet & legs 97
Rear legs, side view 87 Straight Sickled
Rear legs, back rear view 113 Toes out Parallel, bow-legged
Foot angle 101 Low Steep
Bone quality 95 Coarse Fine and thin
Hock quality 87 Filled Dry
Udder 109
Fore udder attachment 118 Loose Strong
Rear udder height 110 Low High
Rear udder width 115 Narrow Wide
Udder support 98 Weak Strong
Udder depth 110 Deep High
Udder balance 108 Deep rear udder Deep front udder
Teat length 103 Short Long
Teat thickness 93 Thin Thick
Teat placement (front) 111 Wide Close
Teat placement (back) 107 Wide Close

NAV proof run date: 05-05-2026 Reliability 94 % Number of daughters: 1420

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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