VH Sheik P - DEU 362851467

Production & Efficiency

Trait Index 80 100 120
Production 123
Milk kg 106
Fat, kg 121
Fat, % 111
Protein kg 118
Protein % 116
Persistency 101
Growth 97
Daily carcass gain 106
Carcass conformation score 89
Saved feed 91
Maintenance efficiency 99
Metabolic efficiency 92

NAV proof run date: 02-04-2024 Reliability 77 % Number of daughters: 0

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 106 196.8 11388
Fat kg, 305 days 121 26.2 464
Fat %, 305 days 111 0.18 4.1
Protein kg, 305 days 118 18.0 396
Protein %, 305 days 116 0.12 3.5

NAV proof run date: 02-04-2024 Reliability 77 % Number of daughters: 0

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 105
Interval from calving to first insemination (cows) 98
Interval from first to last insemination (heifers) 96
Interval from first to last insemination (cows) 106
Number of inseminations (heifers) 98
Number of inseminations (cows) 95
Calving sire 100
Calving maternal 108
Udder health 104
General health 96
Longevity 115
Hoof health 105
Sole Ulcer 104
Sole Hemorrhage 105
Heel Horn Erosion 109
Digital dermatitis + Interdigital Dermatitis 99
Verrucose dermatitis + Interdigital Hyperplasia 99
Double sole + White line separation 104
Cork screw claw 106
Youngstock survival 90

NAV proof run date: 02-04-2024 Reliability 75 % Number of daughters: 0

Functional

Trait Index 80 100 120
Milkability 117
Temperament 116

NAV proof run date: 02-04-2024 Reliability 56 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 107
Stature 117 Short Tall
Body depth 98 Shallow Deep
Chest width 84 Narrow Wide
Rib structure 112 Coarse Angular
Top line 108 Weak Strong
Rump width 111 Narrow pins Wide pins
Rump angle 95 High pins Low pins
Feet & legs 108
Rear legs, side view 97 Straight Sickled
Rear legs, back rear view 107 Toes out Parallel, bow-legged
Foot angle 103 Low Steep
Bone quality 109 Coarse Fine and thin
Hock quality 101 Filled Dry
Udder 116
Fore udder attachment 112 Loose Strong
Rear udder height 123 Low High
Rear udder width 111 Narrow Wide
Udder support 93 Weak Strong
Udder depth 125 Deep High
Udder balance 109 Deep rear udder Deep front udder
Teat length 84 Short Long
Teat thickness 87 Thin Thick
Teat placement (front) 98 Wide Close
Teat placement (back) 108 Wide Close

NAV proof run date: 02-04-2024 Reliability 56 % Number of daughters: 0

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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