VH Zinedin - DEU 770836798

Production & Efficiency

Trait Index 80 100 120
Production 93
Milk kg 85
Fat, kg 100
Fat, % 114
Protein kg 85
Protein % 103
Persistency 112
Growth 109
Daily carcass gain 101
Carcass conformation score 113
Saved feed 90
Maintenance efficiency 103

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 2261

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 85 -492.1 11702
Fat kg, 305 days 100 0.0 483
Fat %, 305 days 114 0.22 4.2
Protein kg, 305 days 85 -15.0 413
Protein %, 305 days 103 0.02 3.5

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 2261

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 123
Interval from calving to first insemination (cows) 116
Interval from first to last insemination (heifers) 104
Interval from first to last insemination (cows) 123
Number of inseminations (heifers) 109
Number of inseminations (cows) 122
Calving sire 108
Calving maternal 104
Udder health 104
General health 117
Longevity 109
Hoof health 114
Sole Ulcer 108
Sole Hemorrhage 96
Heel Horn Erosion 110
Digital dermatitis + Interdigital Dermatitis 123
Verrucose dermatitis + Interdigital Hyperplasia 116
Double sole + White line separation 109
Cork screw claw 88
Youngstock survival 108

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 2015

Functional

Trait Index 80 100 120
Milkability 120
Temperament 98

NAV proof run date: 03-02-2026 Reliability 94 % Number of daughters: 817

Conformation

Trait Index 80 100 120
Frame 89
Stature 87 Short Tall
Body depth 90 Shallow Deep
Chest width 103 Narrow Wide
Rib structure 91 Coarse Angular
Top line 91 Weak Strong
Rump width 95 Narrow pins Wide pins
Rump angle 86 High pins Low pins
Feet & legs 99
Rear legs, side view 105 Straight Sickled
Rear legs, back rear view 81 Toes out Parallel, bow-legged
Foot angle 93 Low Steep
Bone quality 113 Coarse Fine and thin
Hock quality 114 Filled Dry
Udder 106
Fore udder attachment 109 Loose Strong
Rear udder height 95 Low High
Rear udder width 100 Narrow Wide
Udder support 90 Weak Strong
Udder depth 110 Deep High
Udder balance 116 Deep rear udder Deep front udder
Teat length 99 Short Long
Teat thickness 97 Thin Thick
Teat placement (front) 91 Wide Close
Teat placement (back) 90 Wide Close

NAV proof run date: 03-02-2026 Reliability 94 % Number of daughters: 817

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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