VH Zinedin - DEU 770836798

Production & Efficiency

Trait Index 80 100 120
Production 98
Milk kg 88
Fat, kg 105
Fat, % 116
Protein kg 89
Protein % 103
Persistency 112
Growth 111
Daily carcass gain 103
Carcass conformation score 113
Saved feed 95
Maintenance efficiency 104
Metabolic efficiency 91

NAV proof run date: 03-12-2024 Reliability 99 % Number of daughters: 1601

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 88 -393.7 11488
Fat kg, 305 days 105 6.2 470
Fat %, 305 days 116 0.26 4.1
Protein kg, 305 days 89 -11.0 402
Protein %, 305 days 103 0.02 3.5

NAV proof run date: 03-12-2024 Reliability 99 % Number of daughters: 1601

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 117
Interval from calving to first insemination (cows) 110
Interval from first to last insemination (heifers) 107
Interval from first to last insemination (cows) 118
Number of inseminations (heifers) 108
Number of inseminations (cows) 112
Calving sire 108
Calving maternal 102
Udder health 99
General health 120
Longevity 117
Hoof health 112
Sole Ulcer 107
Sole Hemorrhage 97
Heel Horn Erosion 102
Digital dermatitis + Interdigital Dermatitis 122
Verrucose dermatitis + Interdigital Hyperplasia 115
Double sole + White line separation 115
Cork screw claw 87
Youngstock survival 110

NAV proof run date: 03-12-2024 Reliability 97 % Number of daughters: 1467

Functional

Trait Index 80 100 120
Milkability 123
Temperament 99

NAV proof run date: 03-12-2024 Reliability 90 % Number of daughters: 442

Conformation

Trait Index 80 100 120
Frame 91
Stature 89 Short Tall
Body depth 92 Shallow Deep
Chest width 105 Narrow Wide
Rib structure 92 Coarse Angular
Top line 90 Weak Strong
Rump width 93 Narrow pins Wide pins
Rump angle 86 High pins Low pins
Feet & legs 101
Rear legs, side view 107 Straight Sickled
Rear legs, back rear view 82 Toes out Parallel, bow-legged
Foot angle 92 Low Steep
Bone quality 116 Coarse Fine and thin
Hock quality 115 Filled Dry
Udder 110
Fore udder attachment 114 Loose Strong
Rear udder height 97 Low High
Rear udder width 105 Narrow Wide
Udder support 92 Weak Strong
Udder depth 109 Deep High
Udder balance 112 Deep rear udder Deep front udder
Teat length 98 Short Long
Teat thickness 96 Thin Thick
Teat placement (front) 91 Wide Close
Teat placement (back) 91 Wide Close

NAV proof run date: 03-12-2024 Reliability 90 % Number of daughters: 442

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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