VH Raggat - USA 3143383967

Production & Efficiency

Trait Index 80 100 120
Production 112
Milk kg 108
Fat, kg 107
Fat, % 98
Protein kg 115
Protein % 107
Persistency 96
Growth 101
Daily carcass gain 107
Carcass conformation score 96
Saved feed 91
Maintenance efficiency 97

NAV proof run date: 03-11-2026 Reliability 99 % Number of daughters: 414

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 108 262.5 11758
Fat kg, 305 days 107 8.7 487
Fat %, 305 days 98 -0.03 4.2
Protein kg, 305 days 115 15.0 416
Protein %, 305 days 107 0.05 3.6

NAV proof run date: 03-11-2026 Reliability 99 % Number of daughters: 414

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 107
Interval from calving to first insemination (cows) 98
Interval from first to last insemination (heifers) 117
Interval from first to last insemination (cows) 105
Number of inseminations (heifers) 116
Number of inseminations (cows) 109
Calving sire 107
Calving maternal 106
Udder health 98
General health 102
Longevity 105
Hoof health 107
Sole Ulcer 110
Sole Hemorrhage 105
Heel Horn Erosion 100
Digital dermatitis + Interdigital Dermatitis 102
Verrucose dermatitis + Interdigital Hyperplasia 95
Double sole + White line separation 111
Cork screw claw 96
Youngstock survival 86

NAV proof run date: 03-11-2026 Reliability 96 % Number of daughters: 405

Functional

Trait Index 80 100 120
Milkability 83
Temperament 99

NAV proof run date: 03-11-2026 Reliability 91 % Number of daughters: 165

Conformation

Trait Index 80 100 120
Frame 103
Stature 100 Short Tall
Body depth 101 Shallow Deep
Chest width 112 Narrow Wide
Rib structure 89 Coarse Angular
Top line 105 Weak Strong
Rump width 108 Narrow pins Wide pins
Rump angle 86 High pins Low pins
Feet & legs 97
Rear legs, side view 107 Straight Sickled
Rear legs, back rear view 104 Toes out Parallel, bow-legged
Foot angle 85 Low Steep
Bone quality 94 Coarse Fine and thin
Hock quality 100 Filled Dry
Udder 104
Fore udder attachment 114 Loose Strong
Rear udder height 101 Low High
Rear udder width 112 Narrow Wide
Udder support 95 Weak Strong
Udder depth 103 Deep High
Udder balance 109 Deep rear udder Deep front udder
Teat length 109 Short Long
Teat thickness 108 Thin Thick
Teat placement (front) 108 Wide Close
Teat placement (back) 106 Wide Close

NAV proof run date: 03-11-2026 Reliability 91 % Number of daughters: 165

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