VH Slatt P - DNK 260203 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 117
Milk kg 116
Fat, kg 114
Fat, % 99
Protein kg 119
Protein % 102
Persistency 112
Growth 122
Daily carcass gain 133
Carcass conformation score 106
Saved feed 97
Maintenance efficiency 98
Metabolic efficiency 99

NAV proof run date: 07-05-2024 Reliability 98 % Number of daughters: 704

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 116 524.9 11388
Fat kg, 305 days 114 17.5 464
Fat %, 305 days 99 -0.02 4.1
Protein kg, 305 days 119 19.0 396
Protein %, 305 days 102 0.01 3.5

NAV proof run date: 07-05-2024 Reliability 98 % Number of daughters: 704

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 107
Interval from calving to first insemination (cows) 97
Interval from first to last insemination (heifers) 120
Interval from first to last insemination (cows) 105
Number of inseminations (heifers) 118
Number of inseminations (cows) 110
Calving sire 95
Calving maternal 97
Udder health 90
General health 88
Longevity 89
Hoof health 76
Sole Ulcer 88
Sole Hemorrhage 89
Heel Horn Erosion 90
Digital dermatitis + Interdigital Dermatitis 69
Verrucose dermatitis + Interdigital Hyperplasia 65
Double sole + White line separation 87
Cork screw claw 102
Youngstock survival 117

NAV proof run date: 07-05-2024 Reliability 97 % Number of daughters: 691

Functional

Trait Index 80 100 120
Milkability 111
Temperament 108

NAV proof run date: 07-05-2024 Reliability 89 % Number of daughters: 213

Conformation

Trait Index 80 100 120
Frame 108
Stature 111 Short Tall
Body depth 101 Shallow Deep
Chest width 95 Narrow Wide
Rib structure 119 Coarse Angular
Top line 108 Weak Strong
Rump width 100 Narrow pins Wide pins
Rump angle 90 High pins Low pins
Feet & legs 92
Rear legs, side view 109 Straight Sickled
Rear legs, back rear view 95 Toes out Parallel, bow-legged
Foot angle 108 Low Steep
Bone quality 90 Coarse Fine and thin
Hock quality 92 Filled Dry
Udder 107
Fore udder attachment 109 Loose Strong
Rear udder height 123 Low High
Rear udder width 109 Narrow Wide
Udder support 102 Weak Strong
Udder depth 118 Deep High
Udder balance 128 Deep rear udder Deep front udder
Teat length 105 Short Long
Teat thickness 104 Thin Thick
Teat placement (front) 107 Wide Close
Teat placement (back) 120 Wide Close

NAV proof run date: 07-05-2024 Reliability 89 % Number of daughters: 213

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