VH Hjalte - DEU 1262529713

Production & Efficiency

Trait Index 80 100 120
Production 115
Milk kg 113
Fat, kg 117
Fat, % 103
Protein kg 113
Protein % 97
Persistency 99
Growth 100
Daily carcass gain 104
Carcass conformation score 95
Saved feed 95
Maintenance efficiency 99

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 1615

Expected Progeny Difference

Trait Index Bull effect Average
Milk lbs, 305 days 113 940.27 25,798.49
Fat lbs, 305 days 117 46.74 1,064.83
Fat %, 305 days 103 0.05 4.2
Protein lbs, 305 days 113 28.66 910.51
Protein %, 305 days 97 -0.02 3.5

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 1615

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 104
Interval from calving to first insemination (cows) 101
Interval from first to last insemination (heifers) 99
Interval from first to last insemination (cows) 105
Number of inseminations (heifers) 100
Number of inseminations (cows) 103
Calving sire 98
Calving maternal 109
Udder health 108
General health 98
Longevity 105
Hoof health 92
Sole Ulcer 90
Sole Hemorrhage 87
Heel Horn Erosion 93
Digital dermatitis + Interdigital Dermatitis 104
Verrucose dermatitis + Interdigital Hyperplasia 105
Double sole + White line separation 93
Cork screw claw 96
Youngstock survival 96

NAV proof run date: 03-02-2026 Reliability 98 % Number of daughters: 1364

Functional

Trait Index 80 100 120
Milkability 91
Temperament 104

NAV proof run date: 03-02-2026 Reliability 94 % Number of daughters: 777

Conformation

Trait Index 80 100 120
Frame 99
Stature 111 Short Tall
Body depth 94 Shallow Deep
Chest width 89 Narrow Wide
Rib structure 110 Coarse Angular
Top line 105 Weak Strong
Rump width 91 Narrow pins Wide pins
Rump angle 107 High pins Low pins
Feet & legs 112
Rear legs, side view 104 Straight Sickled
Rear legs, back rear view 110 Toes out Parallel, bow-legged
Foot angle 94 Low Steep
Bone quality 110 Coarse Fine and thin
Hock quality 111 Filled Dry
Udder 105
Fore udder attachment 98 Loose Strong
Rear udder height 115 Low High
Rear udder width 113 Narrow Wide
Udder support 109 Weak Strong
Udder depth 105 Deep High
Udder balance 107 Deep rear udder Deep front udder
Teat length 95 Short Long
Teat thickness 93 Thin Thick
Teat placement (front) 110 Wide Close
Teat placement (back) 101 Wide Close

NAV proof run date: 03-02-2026 Reliability 94 % Number of daughters: 777

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/ HH1C Carrier
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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