VH SilaniP - DNK 261907 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 125
Milk kg 110
Fat, kg 129
Fat, % 115
Protein kg 117
Protein % 109
Persistency 124
Growth 97
Daily carcass gain 103
Carcass conformation score 93
Saved feed 93
Maintenance efficiency 99
Metabolic efficiency 94

NAV proof run date: 03-09-2024 Reliability 83 % Number of daughters: 0

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 110 328.1 11437
Fat kg, 305 days 129 36.2 466
Fat %, 305 days 115 0.24 4.1
Protein kg, 305 days 117 17.0 399
Protein %, 305 days 109 0.07 3.5

NAV proof run date: 03-09-2024 Reliability 83 % Number of daughters: 0

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 100
Interval from calving to first insemination (cows) 103
Interval from first to last insemination (heifers) 101
Interval from first to last insemination (cows) 100
Number of inseminations (heifers) 106
Number of inseminations (cows) 102
Calving sire 103
Calving maternal 96
Udder health 96
General health 103
Longevity 100
Hoof health 100
Sole Ulcer 96
Sole Hemorrhage 89
Heel Horn Erosion 103
Digital dermatitis + Interdigital Dermatitis 108
Verrucose dermatitis + Interdigital Hyperplasia 108
Double sole + White line separation 97
Cork screw claw 91
Youngstock survival 94

NAV proof run date: 03-09-2024 Reliability 81 % Number of daughters: 0

Functional

Trait Index 80 100 120
Milkability 90
Temperament 97

NAV proof run date: 03-09-2024 Reliability 64 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 104
Stature 106 Short Tall
Body depth 98 Shallow Deep
Chest width 92 Narrow Wide
Rib structure 104 Coarse Angular
Top line 96 Weak Strong
Rump width 115 Narrow pins Wide pins
Rump angle 99 High pins Low pins
Feet & legs 97
Rear legs, side view 109 Straight Sickled
Rear legs, back rear view 94 Toes out Parallel, bow-legged
Foot angle 97 Low Steep
Bone quality 101 Coarse Fine and thin
Hock quality 107 Filled Dry
Udder 99
Fore udder attachment 94 Loose Strong
Rear udder height 114 Low High
Rear udder width 116 Narrow Wide
Udder support 104 Weak Strong
Udder depth 96 Deep High
Udder balance 85 Deep rear udder Deep front udder
Teat length 104 Short Long
Teat thickness 97 Thin Thick
Teat placement (front) 106 Wide Close
Teat placement (back) 113 Wide Close

NAV proof run date: 03-09-2024 Reliability 64 % 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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