VH Gosh - DNK 261542 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 121
Milk kg 100
Fat, kg 125
Fat, % 120
Protein kg 111
Protein % 116
Persistency 119
Growth 99
Daily carcass gain 101
Carcass conformation score 98
Saved feed 101
Maintenance efficiency 107
Metabolic efficiency 94

NAV proof run date: 02-07-2024 Reliability 82 % Number of daughters: 5

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 100 0.0 11437
Fat kg, 305 days 125 31.2 466
Fat %, 305 days 120 0.32 4.1
Protein kg, 305 days 111 11.0 399
Protein %, 305 days 116 0.12 3.5

NAV proof run date: 02-07-2024 Reliability 82 % Number of daughters: 5

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 105
Interval from calving to first insemination (cows) 94
Interval from first to last insemination (heifers) 119
Interval from first to last insemination (cows) 106
Number of inseminations (heifers) 119
Number of inseminations (cows) 105
Calving sire 101
Calving maternal 101
Udder health 98
General health 101
Longevity 105
Hoof health 112
Sole Ulcer 105
Sole Hemorrhage 105
Heel Horn Erosion 110
Digital dermatitis + Interdigital Dermatitis 117
Verrucose dermatitis + Interdigital Hyperplasia 116
Double sole + White line separation 99
Cork screw claw 104
Youngstock survival 105

NAV proof run date: 02-07-2024 Reliability 81 % Number of daughters: 0

Functional

Trait Index 80 100 120
Milkability 107
Temperament 110

NAV proof run date: 02-07-2024 Reliability 65 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 93
Stature 96 Short Tall
Body depth 98 Shallow Deep
Chest width 90 Narrow Wide
Rib structure 97 Coarse Angular
Top line 99 Weak Strong
Rump width 99 Narrow pins Wide pins
Rump angle 92 High pins Low pins
Feet & legs 103
Rear legs, side view 94 Straight Sickled
Rear legs, back rear view 99 Toes out Parallel, bow-legged
Foot angle 91 Low Steep
Bone quality 113 Coarse Fine and thin
Hock quality 104 Filled Dry
Udder 101
Fore udder attachment 97 Loose Strong
Rear udder height 110 Low High
Rear udder width 109 Narrow Wide
Udder support 99 Weak Strong
Udder depth 101 Deep High
Udder balance 99 Deep rear udder Deep front udder
Teat length 90 Short Long
Teat thickness 89 Thin Thick
Teat placement (front) 94 Wide Close
Teat placement (back) 100 Wide Close

NAV proof run date: 02-07-2024 Reliability 65 % 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/ HH1C Carrier
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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