VH Fillman - DNK 260947 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 122
Milk kg 106
Fat, kg 114
Fat, % 106
Protein kg 122
Protein % 121
Persistency 107
Growth 100
Daily carcass gain 112
Carcass conformation score 92
Saved feed 103
Maintenance efficiency 98
Metabolic efficiency 105

NAV proof run date: 04-01-2022 Reliability 79 % Number of daughters: 0

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 106 196.8 11335
Fat kg, 305 days 114 17.5 458
Fat %, 305 days 106 0.10 4.1
Protein kg, 305 days 122 22.0 392
Protein %, 305 days 121 0.15 3.5

NAV proof run date: 04-01-2022 Reliability 79 % Number of daughters: 0

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 113
Calving sire 94
Calving maternal 121
Udder health 109
General health 109
Longevity 113
Hoof health 112
Youngstock survival 100

NAV proof run date: 04-01-2022 Reliability 77 % Number of daughters: 0

Functional

Trait Index 80 100 120
Milkability 97
Temperament 108

NAV proof run date: 04-01-2022 Reliability 68 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 104
Stature 107 Short Tall
Body depth 92 Shallow Deep
Chest width 100 Narrow Wide
Dairy form 105 Coarse Angular
Top line 108 Weak Strong
Rump width 110 Narrow pins Wide pins
Rump angle 79 High pins Low pins
Feet & legs 94
Rear legs, side view 104 Straight Sickled
Rear legs, back rear view 102 Toes out Parallel, bow-legged
Foot angle 96 Low Steep
Bone quality 94 Coarse Fine and thin
Hock quality 92 Filled Dry
Udder 117
Fore udder attachment 106 Loose Strong
Rear udder height 120 Low High
Rear udder width 111 Narrow Wide
Udder support 105 Weak Strong
Udder depth 117 Deep High
Udder balance 101 Deep rear udder Deep front udder
Teat length 107 Short Long
Teat thickness 105 Thin Thick
Teat placement (front) 115 Wide Close
Teat placement (back) 104 Wide Close

NAV proof run date: 04-01-2022 Reliability 68 % 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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