VH SlyPPRC - DEU 362637928

Production & Efficiency

Trait Index 80 100 120
Production 119
Milk kg 114
Fat, kg 111
Fat, % 97
Protein kg 123
Protein % 108
Persistency 118
Growth 101
Daily carcass gain 91
Carcass conformation score 109
Saved feed 92
Maintenance efficiency 98

NAV proof run date: 06-05-2025 Reliability 98 % Number of daughters: 2547

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 114 459.3 11540
Fat kg, 305 days 111 13.7 472
Fat %, 305 days 97 -0.05 4.1
Protein kg, 305 days 123 23.0 404
Protein %, 305 days 108 0.06 3.5

NAV proof run date: 06-05-2025 Reliability 98 % Number of daughters: 2547

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 112
Interval from calving to first insemination (cows) 100
Interval from first to last insemination (heifers) 109
Interval from first to last insemination (cows) 111
Number of inseminations (heifers) 108
Number of inseminations (cows) 110
Calving sire 103
Calving maternal 101
Udder health 92
General health 103
Longevity 114
Hoof health 107
Sole Ulcer 106
Sole Hemorrhage 98
Heel Horn Erosion 106
Digital dermatitis + Interdigital Dermatitis 101
Verrucose dermatitis + Interdigital Hyperplasia 106
Double sole + White line separation 110
Cork screw claw 100
Youngstock survival 94

NAV proof run date: 06-05-2025 Reliability 98 % Number of daughters: 2061

Functional

Trait Index 80 100 120
Milkability 111
Temperament 105

NAV proof run date: 06-05-2025 Reliability 91 % Number of daughters: 579

Conformation

Trait Index 80 100 120
Frame 102
Stature 102 Short Tall
Body depth 97 Shallow Deep
Chest width 109 Narrow Wide
Rib structure 97 Coarse Angular
Top line 103 Weak Strong
Rump width 99 Narrow pins Wide pins
Rump angle 105 High pins Low pins
Feet & legs 96
Rear legs, side view 92 Straight Sickled
Rear legs, back rear view 99 Toes out Parallel, bow-legged
Foot angle 116 Low Steep
Bone quality 89 Coarse Fine and thin
Hock quality 91 Filled Dry
Udder 100
Fore udder attachment 102 Loose Strong
Rear udder height 98 Low High
Rear udder width 98 Narrow Wide
Udder support 92 Weak Strong
Udder depth 103 Deep High
Udder balance 99 Deep rear udder Deep front udder
Teat length 100 Short Long
Teat thickness 86 Thin Thick
Teat placement (front) 77 Wide Close
Teat placement (back) 95 Wide Close

NAV proof run date: 06-05-2025 Reliability 91 % Number of daughters: 579

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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