VH Connect - DEU 363274053

Production & Efficiency

Trait Index 80 100 120
Production 125
Milk kg 125
Fat, kg 122
Fat, % 97
Protein kg 127
Protein % 97
Persistency 105
Growth 86
Daily carcass gain 90
Carcass conformation score 86
Saved feed 110
Maintenance efficiency 95

NAV proof run date: 01-07-2025 Reliability 95 % Number of daughters: 342

Expected Progeny Difference

Trait Index Bull effect Average
Milk lbs, 305 days 125 1,808.23 25,441.35
Fat lbs, 305 days 122 60.63 1,040.58
Fat %, 305 days 97 -0.05 4.1
Protein lbs, 305 days 127 59.52 890.67
Protein %, 305 days 97 -0.02 3.5

NAV proof run date: 01-07-2025 Reliability 95 % Number of daughters: 342

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 97
Interval from calving to first insemination (cows) 89
Interval from first to last insemination (heifers) 106
Interval from first to last insemination (cows) 99
Number of inseminations (heifers) 107
Number of inseminations (cows) 101
Calving sire 96
Calving maternal 103
Udder health 94
General health 105
Longevity 109
Hoof health 104
Sole Ulcer 92
Sole Hemorrhage 95
Heel Horn Erosion 120
Digital dermatitis + Interdigital Dermatitis 118
Verrucose dermatitis + Interdigital Hyperplasia 118
Double sole + White line separation 91
Cork screw claw 105
Youngstock survival 87

NAV proof run date: 01-07-2025 Reliability 84 % Number of daughters: 213

Functional

Trait Index 80 100 120
Milkability 115
Temperament 120

NAV proof run date: 01-07-2025 Reliability 77 % Number of daughters: 38

Conformation

Trait Index 80 100 120
Frame 108
Stature 100 Short Tall
Body depth 105 Shallow Deep
Chest width 101 Narrow Wide
Rib structure 113 Coarse Angular
Top line 88 Weak Strong
Rump width 108 Narrow pins Wide pins
Rump angle 91 High pins Low pins
Feet & legs 98
Rear legs, side view 99 Straight Sickled
Rear legs, back rear view 99 Toes out Parallel, bow-legged
Foot angle 100 Low Steep
Bone quality 99 Coarse Fine and thin
Hock quality 98 Filled Dry
Udder 92
Fore udder attachment 106 Loose Strong
Rear udder height 104 Low High
Rear udder width 105 Narrow Wide
Udder support 97 Weak Strong
Udder depth 108 Deep High
Udder balance 127 Deep rear udder Deep front udder
Teat length 95 Short Long
Teat thickness 102 Thin Thick
Teat placement (front) 107 Wide Close
Teat placement (back) 114 Wide Close

NAV proof run date: 01-07-2025 Reliability 77 % Number of daughters: 38

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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