VH Sheik P - DEU 362851467

Production & Efficiency

Trait Index 80 100 120
Production 120
Milk kg 111
Fat, kg 118
Fat, % 105
Protein kg 118
Protein % 107
Persistency 94
Growth 97
Daily carcass gain 103
Carcass conformation score 92
Saved feed 113
Maintenance efficiency 109

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 6971

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 111 360.9 11758
Fat kg, 305 days 118 22.5 487
Fat %, 305 days 105 0.08 4.2
Protein kg, 305 days 118 18.0 416
Protein %, 305 days 107 0.05 3.6

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 6971

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 106
Interval from calving to first insemination (cows) 102
Interval from first to last insemination (heifers) 111
Interval from first to last insemination (cows) 104
Number of inseminations (heifers) 114
Number of inseminations (cows) 106
Calving sire 100
Calving maternal 108
Udder health 92
General health 87
Longevity 105
Hoof health 103
Sole Ulcer 105
Sole Hemorrhage 104
Heel Horn Erosion 105
Digital dermatitis + Interdigital Dermatitis 90
Verrucose dermatitis + Interdigital Hyperplasia 103
Double sole + White line separation 99
Cork screw claw 101
Youngstock survival 88

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 6040

Functional

Trait Index 80 100 120
Milkability 123
Temperament 113

NAV proof run date: 05-05-2026 Reliability 96 % Number of daughters: 2324

Conformation

Trait Index 80 100 120
Frame 101
Stature 112 Short Tall
Body depth 92 Shallow Deep
Chest width 78 Narrow Wide
Rib structure 108 Coarse Angular
Top line 106 Weak Strong
Rump width 114 Narrow pins Wide pins
Rump angle 98 High pins Low pins
Feet & legs 105
Rear legs, side view 94 Straight Sickled
Rear legs, back rear view 103 Toes out Parallel, bow-legged
Foot angle 104 Low Steep
Bone quality 108 Coarse Fine and thin
Hock quality 103 Filled Dry
Udder 103
Fore udder attachment 106 Loose Strong
Rear udder height 120 Low High
Rear udder width 109 Narrow Wide
Udder support 88 Weak Strong
Udder depth 121 Deep High
Udder balance 114 Deep rear udder Deep front udder
Teat length 83 Short Long
Teat thickness 89 Thin Thick
Teat placement (front) 98 Wide Close
Teat placement (back) 106 Wide Close

NAV proof run date: 05-05-2026 Reliability 96 % Number of daughters: 2324

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