VH SlyPPRC - DEU 362637928

Production & Efficiency

Trait Index 80 100 120
Production 114
Milk kg 113
Fat, kg 109
Fat, % 97
Protein kg 118
Protein % 105
Persistency 130
Growth 100
Daily carcass gain 88
Carcass conformation score 109
Saved feed 96
Maintenance efficiency 96

NAV proof run date: 01-04-2025 Reliability 98 % Number of daughters: 1347

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 113 426.5 11540
Fat kg, 305 days 109 11.2 472
Fat %, 305 days 97 -0.05 4.1
Protein kg, 305 days 118 18.0 404
Protein %, 305 days 105 0.04 3.5

NAV proof run date: 01-04-2025 Reliability 98 % Number of daughters: 1347

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 109
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 102
Udder health 90
General health 102
Longevity 115
Hoof health 106
Sole Ulcer 106
Sole Hemorrhage 98
Heel Horn Erosion 102
Digital dermatitis + Interdigital Dermatitis 101
Verrucose dermatitis + Interdigital Hyperplasia 109
Double sole + White line separation 110
Cork screw claw 93
Youngstock survival 96

NAV proof run date: 01-04-2025 Reliability 96 % Number of daughters: 1006

Functional

Trait Index 80 100 120
Milkability 111
Temperament 101

NAV proof run date: 01-04-2025 Reliability 89 % Number of daughters: 250

Conformation

Trait Index 80 100 120
Frame 102
Stature 102 Short Tall
Body depth 96 Shallow Deep
Chest width 108 Narrow Wide
Rib structure 95 Coarse Angular
Top line 104 Weak Strong
Rump width 102 Narrow pins Wide pins
Rump angle 104 High pins Low pins
Feet & legs 95
Rear legs, side view 90 Straight Sickled
Rear legs, back rear view 98 Toes out Parallel, bow-legged
Foot angle 118 Low Steep
Bone quality 90 Coarse Fine and thin
Hock quality 89 Filled Dry
Udder 103
Fore udder attachment 104 Loose Strong
Rear udder height 96 Low High
Rear udder width 98 Narrow Wide
Udder support 94 Weak Strong
Udder depth 104 Deep High
Udder balance 96 Deep rear udder Deep front udder
Teat length 100 Short Long
Teat thickness 82 Thin Thick
Teat placement (front) 76 Wide Close
Teat placement (back) 95 Wide Close

NAV proof run date: 01-04-2025 Reliability 89 % Number of daughters: 250

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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