VH Starwar - DEU 363456320

Production & Efficiency

Trait Index 80 100 120
Production 125
Milk kg 133
Fat, kg 119
Fat, % 90
Protein kg 132
Protein % 93
Persistency 124
Growth 119
Daily carcass gain 113
Carcass conformation score 117
Saved feed 101
Maintenance efficiency 108

NAV proof run date: 05-05-2026 Reliability 90 % Number of daughters: 2

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 133 1082.6 11758
Fat kg, 305 days 119 23.7 487
Fat %, 305 days 90 -0.16 4.2
Protein kg, 305 days 132 32.0 416
Protein %, 305 days 93 -0.05 3.6

NAV proof run date: 05-05-2026 Reliability 90 % Number of daughters: 2

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 102
Interval from calving to first insemination (cows) 101
Interval from first to last insemination (heifers) 105
Interval from first to last insemination (cows) 102
Number of inseminations (heifers) 98
Number of inseminations (cows) 99
Calving sire 102
Calving maternal 100
Udder health 105
General health 89
Longevity 108
Hoof health 114
Sole Ulcer 107
Sole Hemorrhage 106
Heel Horn Erosion 119
Digital dermatitis + Interdigital Dermatitis 120
Verrucose dermatitis + Interdigital Hyperplasia 107
Double sole + White line separation 98
Cork screw claw 106
Youngstock survival 95

NAV proof run date: 05-05-2026 Reliability 80 % Number of daughters: 1

Functional

Trait Index 80 100 120
Milkability 85
Temperament 82

NAV proof run date: 05-05-2026 Reliability 61 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 95
Stature 82 Short Tall
Body depth 100 Shallow Deep
Chest width 109 Narrow Wide
Rib structure 95 Coarse Angular
Top line 92 Weak Strong
Rump width 104 Narrow pins Wide pins
Rump angle 80 High pins Low pins
Feet & legs 98
Rear legs, side view 86 Straight Sickled
Rear legs, back rear view 105 Toes out Parallel, bow-legged
Foot angle 106 Low Steep
Bone quality 99 Coarse Fine and thin
Hock quality 92 Filled Dry
Udder 100
Fore udder attachment 99 Loose Strong
Rear udder height 117 Low High
Rear udder width 106 Narrow Wide
Udder support 102 Weak Strong
Udder depth 94 Deep High
Udder balance 101 Deep rear udder Deep front udder
Teat length 106 Short Long
Teat thickness 95 Thin Thick
Teat placement (front) 101 Wide Close
Teat placement (back) 97 Wide Close

NAV proof run date: 05-05-2026 Reliability 61 % Number of daughters: 0

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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