VH Putur - DNK 261904 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 121
Milk kg 101
Fat, kg 121
Fat, % 116
Protein kg 114
Protein % 118
Persistency 101
Growth 96
Daily carcass gain 101
Carcass conformation score 92
Saved feed 97
Maintenance efficiency 92

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 3089

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 101 32.8 11633
Fat kg, 305 days 121 26.2 477
Fat %, 305 days 116 0.26 4.2
Protein kg, 305 days 114 14.0 409
Protein %, 305 days 118 0.13 3.5

NAV proof run date: 04-11-2025 Reliability 99 % Number of daughters: 3089

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 113
Interval from calving to first insemination (cows) 116
Interval from first to last insemination (heifers) 91
Interval from first to last insemination (cows) 115
Number of inseminations (heifers) 95
Number of inseminations (cows) 108
Calving sire 93
Calving maternal 98
Udder health 101
General health 109
Longevity 100
Hoof health 101
Sole Ulcer 100
Sole Hemorrhage 110
Heel Horn Erosion 95
Digital dermatitis + Interdigital Dermatitis 108
Verrucose dermatitis + Interdigital Hyperplasia 92
Double sole + White line separation 97
Cork screw claw 109
Youngstock survival 92

NAV proof run date: 04-11-2025 Reliability 98 % Number of daughters: 2675

Functional

Trait Index 80 100 120
Milkability 114
Temperament 103

NAV proof run date: 04-11-2025 Reliability 89 % Number of daughters: 779

Conformation

Trait Index 80 100 120
Frame 117
Stature 112 Short Tall
Body depth 112 Shallow Deep
Chest width 103 Narrow Wide
Rib structure 116 Coarse Angular
Top line 109 Weak Strong
Rump width 114 Narrow pins Wide pins
Rump angle 110 High pins Low pins
Feet & legs 97
Rear legs, side view 89 Straight Sickled
Rear legs, back rear view 111 Toes out Parallel, bow-legged
Foot angle 100 Low Steep
Bone quality 94 Coarse Fine and thin
Hock quality 88 Filled Dry
Udder 109
Fore udder attachment 117 Loose Strong
Rear udder height 112 Low High
Rear udder width 114 Narrow Wide
Udder support 99 Weak Strong
Udder depth 109 Deep High
Udder balance 110 Deep rear udder Deep front udder
Teat length 103 Short Long
Teat thickness 95 Thin Thick
Teat placement (front) 110 Wide Close
Teat placement (back) 106 Wide Close

NAV proof run date: 04-11-2025 Reliability 89 % Number of daughters: 779

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