VH Sheik P - DEU 362851467

Production & Efficiency

Trait Index 80 100 120
Production 112
Milk kg 109
Fat, kg 111
Fat, % 102
Protein kg 111
Protein % 102
Persistency 94
Growth 95
Daily carcass gain 103
Carcass conformation score 88
Saved feed 99
Maintenance efficiency 101

NAV proof run date: 01-04-2025 Reliability 95 % Number of daughters: 539

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 109 295.3 11540
Fat kg, 305 days 111 13.7 472
Fat %, 305 days 102 0.03 4.1
Protein kg, 305 days 111 11.0 404
Protein %, 305 days 102 0.01 3.5

NAV proof run date: 01-04-2025 Reliability 95 % Number of daughters: 539

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 103
Interval from calving to first insemination (cows) 94
Interval from first to last insemination (heifers) 110
Interval from first to last insemination (cows) 106
Number of inseminations (heifers) 113
Number of inseminations (cows) 109
Calving sire 101
Calving maternal 110
Udder health 86
General health 81
Longevity 113
Hoof health 100
Sole Ulcer 103
Sole Hemorrhage 96
Heel Horn Erosion 101
Digital dermatitis + Interdigital Dermatitis 94
Verrucose dermatitis + Interdigital Hyperplasia 97
Double sole + White line separation 100
Cork screw claw 97
Youngstock survival 90

NAV proof run date: 01-04-2025 Reliability 89 % Number of daughters: 314

Functional

Trait Index 80 100 120
Milkability 123
Temperament 120

NAV proof run date: 01-04-2025 Reliability 82 % Number of daughters: 101

Conformation

Trait Index 80 100 120
Frame 108
Stature 117 Short Tall
Body depth 98 Shallow Deep
Chest width 82 Narrow Wide
Rib structure 113 Coarse Angular
Top line 107 Weak Strong
Rump width 114 Narrow pins Wide pins
Rump angle 97 High pins Low pins
Feet & legs 110
Rear legs, side view 91 Straight Sickled
Rear legs, back rear view 112 Toes out Parallel, bow-legged
Foot angle 105 Low Steep
Bone quality 107 Coarse Fine and thin
Hock quality 105 Filled Dry
Udder 107
Fore udder attachment 113 Loose Strong
Rear udder height 122 Low High
Rear udder width 111 Narrow Wide
Udder support 94 Weak Strong
Udder depth 121 Deep High
Udder balance 109 Deep rear udder Deep front udder
Teat length 81 Short Long
Teat thickness 84 Thin Thick
Teat placement (front) 100 Wide Close
Teat placement (back) 109 Wide Close

NAV proof run date: 01-04-2025 Reliability 82 % Number of daughters: 101

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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