VH Hjalte - DEU 1262529713

Production & Efficiency

Trait Index 80 100 120
Production 119
Milk kg 113
Fat, kg 120
Fat, % 105
Protein kg 115
Protein % 101
Persistency 102
Growth 98
Daily carcass gain 103
Carcass conformation score 94
Saved feed 87
Maintenance efficiency 97
Metabolic efficiency 90

NAV proof run date: 03-12-2024 Reliability 94 % Number of daughters: 373

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 113 426.5 11488
Fat kg, 305 days 120 25.0 470
Fat %, 305 days 105 0.08 4.1
Protein kg, 305 days 115 15.0 402
Protein %, 305 days 101 0.01 3.5

NAV proof run date: 03-12-2024 Reliability 94 % Number of daughters: 373

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 108
Interval from calving to first insemination (cows) 103
Interval from first to last insemination (heifers) 101
Interval from first to last insemination (cows) 109
Number of inseminations (heifers) 99
Number of inseminations (cows) 107
Calving sire 99
Calving maternal 109
Udder health 116
General health 101
Longevity 109
Hoof health 92
Sole Ulcer 91
Sole Hemorrhage 86
Heel Horn Erosion 96
Digital dermatitis + Interdigital Dermatitis 101
Verrucose dermatitis + Interdigital Hyperplasia 103
Double sole + White line separation 88
Cork screw claw 96
Youngstock survival 94

NAV proof run date: 03-12-2024 Reliability 87 % Number of daughters: 263

Functional

Trait Index 80 100 120
Milkability 94
Temperament 96

NAV proof run date: 03-12-2024 Reliability 82 % Number of daughters: 86

Conformation

Trait Index 80 100 120
Frame 100
Stature 112 Short Tall
Body depth 96 Shallow Deep
Chest width 84 Narrow Wide
Rib structure 116 Coarse Angular
Top line 105 Weak Strong
Rump width 90 Narrow pins Wide pins
Rump angle 104 High pins Low pins
Feet & legs 109
Rear legs, side view 110 Straight Sickled
Rear legs, back rear view 106 Toes out Parallel, bow-legged
Foot angle 91 Low Steep
Bone quality 109 Coarse Fine and thin
Hock quality 113 Filled Dry
Udder 103
Fore udder attachment 97 Loose Strong
Rear udder height 115 Low High
Rear udder width 118 Narrow Wide
Udder support 111 Weak Strong
Udder depth 104 Deep High
Udder balance 101 Deep rear udder Deep front udder
Teat length 94 Short Long
Teat thickness 89 Thin Thick
Teat placement (front) 111 Wide Close
Teat placement (back) 106 Wide Close

NAV proof run date: 03-12-2024 Reliability 82 % Number of daughters: 86

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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