VH Sheik P - DEU 99788 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 126
Milk kg 117
Fat, kg 125
Fat, % 106
Protein kg 124
Protein % 106
Persistency 99
Growth 97
Daily carcass gain 104
Carcass conformation score 90
Saved feed 104
Maintenance efficiency 108

NAV proof run date: 02-09-2025 Reliability 100 % Number of daughters: 2906

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 117 557.7 11600
Fat kg, 305 days 125 31.2 475
Fat %, 305 days 106 0.10 4.1
Protein kg, 305 days 124 24.0 406
Protein %, 305 days 106 0.04 3.5

NAV proof run date: 02-09-2025 Reliability 100 % Number of daughters: 2906

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 107
Interval from calving to first insemination (cows) 101
Interval from first to last insemination (heifers) 111
Interval from first to last insemination (cows) 106
Number of inseminations (heifers) 114
Number of inseminations (cows) 110
Calving sire 100
Calving maternal 110
Udder health 90
General health 83
Longevity 113
Hoof health 102
Sole Ulcer 102
Sole Hemorrhage 102
Heel Horn Erosion 108
Digital dermatitis + Interdigital Dermatitis 92
Verrucose dermatitis + Interdigital Hyperplasia 101
Double sole + White line separation 100
Cork screw claw 102
Youngstock survival 88

NAV proof run date: 02-09-2025 Reliability 98 % Number of daughters: 1517

Functional

Trait Index 80 100 120
Milkability 123
Temperament 109

NAV proof run date: 02-09-2025 Reliability 90 % Number of daughters: 827

Conformation

Trait Index 80 100 120
Frame 102
Stature 113 Short Tall
Body depth 92 Shallow Deep
Chest width 77 Narrow Wide
Rib structure 109 Coarse Angular
Top line 107 Weak Strong
Rump width 114 Narrow pins Wide pins
Rump angle 98 High pins Low pins
Feet & legs 109
Rear legs, side view 92 Straight Sickled
Rear legs, back rear view 107 Toes out Parallel, bow-legged
Foot angle 110 Low Steep
Bone quality 107 Coarse Fine and thin
Hock quality 103 Filled Dry
Udder 104
Fore udder attachment 109 Loose Strong
Rear udder height 123 Low High
Rear udder width 109 Narrow Wide
Udder support 88 Weak Strong
Udder depth 122 Deep High
Udder balance 110 Deep rear udder Deep front udder
Teat length 83 Short Long
Teat thickness 86 Thin Thick
Teat placement (front) 96 Wide Close
Teat placement (back) 109 Wide Close

NAV proof run date: 02-09-2025 Reliability 90 % Number of daughters: 827

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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