VH Zinedin - DEU 770836798

Production & Efficiency

Trait Index 80 100 120
Production 101
Milk kg 90
Fat, kg 107
Fat, % 115
Protein kg 92
Protein % 105
Persistency 105
Growth 111
Daily carcass gain 106
Carcass conformation score 113
Saved feed 101
Maintenance efficiency 116
Metabolic efficiency 85

NAV proof run date: 02-04-2024 Reliability 86 % Number of daughters: 82

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 90 -328.1 11388
Fat kg, 305 days 107 8.7 464
Fat %, 305 days 115 0.24 4.1
Protein kg, 305 days 92 -8.0 396
Protein %, 305 days 105 0.04 3.5

NAV proof run date: 02-04-2024 Reliability 86 % Number of daughters: 82

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 114
Interval from calving to first insemination (cows) 103
Interval from first to last insemination (heifers) 107
Interval from first to last insemination (cows) 115
Number of inseminations (heifers) 107
Number of inseminations (cows) 106
Calving sire 108
Calving maternal 102
Udder health 100
General health 120
Longevity 118
Hoof health 108
Sole Ulcer 106
Sole Hemorrhage 100
Heel Horn Erosion 96
Digital dermatitis + Interdigital Dermatitis 110
Verrucose dermatitis + Interdigital Hyperplasia 113
Double sole + White line separation 113
Cork screw claw 86
Youngstock survival 113

NAV proof run date: 02-04-2024 Reliability 83 % Number of daughters: 2

Functional

Trait Index 80 100 120
Milkability 121
Temperament 104

NAV proof run date: 02-04-2024 Reliability 66 % Number of daughters: 9

Conformation

Trait Index 80 100 120
Frame 89
Stature 87 Short Tall
Body depth 94 Shallow Deep
Chest width 95 Narrow Wide
Rib structure 96 Coarse Angular
Top line 89 Weak Strong
Rump width 97 Narrow pins Wide pins
Rump angle 93 High pins Low pins
Feet & legs 102
Rear legs, side view 109 Straight Sickled
Rear legs, back rear view 86 Toes out Parallel, bow-legged
Foot angle 92 Low Steep
Bone quality 116 Coarse Fine and thin
Hock quality 119 Filled Dry
Udder 105
Fore udder attachment 109 Loose Strong
Rear udder height 98 Low High
Rear udder width 108 Narrow Wide
Udder support 92 Weak Strong
Udder depth 109 Deep High
Udder balance 111 Deep rear udder Deep front udder
Teat length 92 Short Long
Teat thickness 86 Thin Thick
Teat placement (front) 91 Wide Close
Teat placement (back) 91 Wide Close

NAV proof run date: 02-04-2024 Reliability 66 % Number of daughters: 9

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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