VH Sheik P - DEU 362851467

Production & Efficiency

Trait Index 80 100 120
Production 121
Milk kg 111
Fat, kg 119
Fat, % 106
Protein kg 118
Protein % 107
Persistency 96
Growth 97
Daily carcass gain 103
Carcass conformation score 91
Saved feed 112
Maintenance efficiency 109

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 5726

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 111 360.9 11702
Fat kg, 305 days 119 23.7 483
Fat %, 305 days 106 0.10 4.2
Protein kg, 305 days 118 18.0 413
Protein %, 305 days 107 0.05 3.5

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 5726

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 105
Interval from calving to first insemination (cows) 101
Interval from first to last insemination (heifers) 111
Interval from first to last insemination (cows) 103
Number of inseminations (heifers) 114
Number of inseminations (cows) 107
Calving sire 100
Calving maternal 110
Udder health 89
General health 85
Longevity 114
Hoof health 103
Sole Ulcer 104
Sole Hemorrhage 103
Heel Horn Erosion 108
Digital dermatitis + Interdigital Dermatitis 89
Verrucose dermatitis + Interdigital Hyperplasia 103
Double sole + White line separation 97
Cork screw claw 101
Youngstock survival 88

NAV proof run date: 03-02-2026 Reliability 99 % Number of daughters: 4805

Functional

Trait Index 80 100 120
Milkability 124
Temperament 113

NAV proof run date: 03-02-2026 Reliability 95 % Number of daughters: 1795

Conformation

Trait Index 80 100 120
Frame 101
Stature 113 Short Tall
Body depth 91 Shallow Deep
Chest width 78 Narrow Wide
Rib structure 109 Coarse Angular
Top line 105 Weak Strong
Rump width 111 Narrow pins Wide pins
Rump angle 99 High pins Low pins
Feet & legs 105
Rear legs, side view 94 Straight Sickled
Rear legs, back rear view 102 Toes out Parallel, bow-legged
Foot angle 106 Low Steep
Bone quality 108 Coarse Fine and thin
Hock quality 102 Filled Dry
Udder 103
Fore udder attachment 107 Loose Strong
Rear udder height 121 Low High
Rear udder width 110 Narrow Wide
Udder support 89 Weak Strong
Udder depth 122 Deep High
Udder balance 113 Deep rear udder Deep front udder
Teat length 82 Short Long
Teat thickness 85 Thin Thick
Teat placement (front) 98 Wide Close
Teat placement (back) 108 Wide Close

NAV proof run date: 03-02-2026 Reliability 95 % Number of daughters: 1795

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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