VH Zinedin - DEU 770836798

Production & Efficiency

Trait Index 80 100 120
Production 97
Milk kg 86
Fat, kg 105
Fat, % 118
Protein kg 86
Protein % 103
Persistency 115
Growth 111
Daily carcass gain 105
Carcass conformation score 113
Saved feed 94
Maintenance efficiency 110
Metabolic efficiency 84

NAV proof run date: 02-07-2024 Reliability 96 % Number of daughters: 551

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 86 -459.3 11437
Fat kg, 305 days 105 6.2 466
Fat %, 305 days 118 0.29 4.1
Protein kg, 305 days 86 -14.0 399
Protein %, 305 days 103 0.02 3.5

NAV proof run date: 02-07-2024 Reliability 96 % Number of daughters: 551

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 111
Interval from calving to first insemination (cows) 104
Interval from first to last insemination (heifers) 105
Interval from first to last insemination (cows) 115
Number of inseminations (heifers) 106
Number of inseminations (cows) 106
Calving sire 108
Calving maternal 102
Udder health 100
General health 121
Longevity 119
Hoof health 109
Sole Ulcer 105
Sole Hemorrhage 97
Heel Horn Erosion 101
Digital dermatitis + Interdigital Dermatitis 115
Verrucose dermatitis + Interdigital Hyperplasia 111
Double sole + White line separation 116
Cork screw claw 85
Youngstock survival 112

NAV proof run date: 02-07-2024 Reliability 90 % Number of daughters: 404

Functional

Trait Index 80 100 120
Milkability 125
Temperament 101

NAV proof run date: 02-07-2024 Reliability 84 % Number of daughters: 97

Conformation

Trait Index 80 100 120
Frame 86
Stature 88 Short Tall
Body depth 88 Shallow Deep
Chest width 98 Narrow Wide
Rib structure 91 Coarse Angular
Top line 89 Weak Strong
Rump width 91 Narrow pins Wide pins
Rump angle 92 High pins Low pins
Feet & legs 101
Rear legs, side view 110 Straight Sickled
Rear legs, back rear view 83 Toes out Parallel, bow-legged
Foot angle 88 Low Steep
Bone quality 122 Coarse Fine and thin
Hock quality 120 Filled Dry
Udder 111
Fore udder attachment 116 Loose Strong
Rear udder height 98 Low High
Rear udder width 103 Narrow Wide
Udder support 93 Weak Strong
Udder depth 115 Deep High
Udder balance 113 Deep rear udder Deep front udder
Teat length 95 Short Long
Teat thickness 91 Thin Thick
Teat placement (front) 93 Wide Close
Teat placement (back) 92 Wide Close

NAV proof run date: 02-07-2024 Reliability 84 % Number of daughters: 97

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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