VH Sheik P - DEU 362851467

Production & Efficiency

Trait Index 80 100 120
Production 128
Milk kg 119
Fat, kg 127
Fat, % 106
Protein kg 126
Protein % 106
Persistency 102
Growth 96
Daily carcass gain 104
Carcass conformation score 89
Saved feed 98
Maintenance efficiency 109

NAV proof run date: 06-05-2025 Reliability 97 % Number of daughters: 1528

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 119 623.3 11540
Fat kg, 305 days 127 33.7 472
Fat %, 305 days 106 0.10 4.1
Protein kg, 305 days 126 26.0 404
Protein %, 305 days 106 0.04 3.5

NAV proof run date: 06-05-2025 Reliability 97 % Number of daughters: 1528

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 106
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 100
Calving maternal 110
Udder health 91
General health 82
Longevity 113
Hoof health 96
Sole Ulcer 97
Sole Hemorrhage 93
Heel Horn Erosion 104
Digital dermatitis + Interdigital Dermatitis 93
Verrucose dermatitis + Interdigital Hyperplasia 99
Double sole + White line separation 95
Cork screw claw 94
Youngstock survival 89

NAV proof run date: 06-05-2025 Reliability 96 % Number of daughters: 1085

Functional

Trait Index 80 100 120
Milkability 122
Temperament 104

NAV proof run date: 06-05-2025 Reliability 89 % Number of daughters: 371

Conformation

Trait Index 80 100 120
Frame 102
Stature 114 Short Tall
Body depth 91 Shallow Deep
Chest width 76 Narrow Wide
Rib structure 111 Coarse Angular
Top line 106 Weak Strong
Rump width 115 Narrow pins Wide pins
Rump angle 98 High pins Low pins
Feet & legs 108
Rear legs, side view 90 Straight Sickled
Rear legs, back rear view 109 Toes out Parallel, bow-legged
Foot angle 106 Low Steep
Bone quality 108 Coarse Fine and thin
Hock quality 102 Filled Dry
Udder 105
Fore udder attachment 108 Loose Strong
Rear udder height 124 Low High
Rear udder width 112 Narrow Wide
Udder support 89 Weak Strong
Udder depth 121 Deep High
Udder balance 108 Deep rear udder Deep front udder
Teat length 81 Short Long
Teat thickness 84 Thin Thick
Teat placement (front) 97 Wide Close
Teat placement (back) 109 Wide Close

NAV proof run date: 06-05-2025 Reliability 89 % Number of daughters: 371

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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