VH Mulan P - DNK 262801 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 119
Milk kg 115
Fat, kg 119
Fat, % 103
Protein kg 118
Protein % 100
Persistency 102
Growth 104
Daily carcass gain 116
Carcass conformation score 92
Saved feed 93
Maintenance efficiency 89

NAV proof run date: 04-11-2025 Reliability 89 % Number of daughters: 0

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 115 492.1 11600
Fat kg, 305 days 119 23.7 475
Fat %, 305 days 103 0.05 4.1
Protein kg, 305 days 118 18.0 406
Protein %, 305 days 100 0.00 3.5

NAV proof run date: 04-11-2025 Reliability 89 % Number of daughters: 0

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 97
Interval from first to last insemination (heifers) 100
Number of inseminations (heifers) 103
Number of inseminations (cows) 102
Calving sire 103
Calving maternal 102
Udder health 100
General health 97
Longevity 108
Hoof health 105
Sole Ulcer 101
Sole Hemorrhage 98
Heel Horn Erosion 105
Digital dermatitis + Interdigital Dermatitis 109
Verrucose dermatitis + Interdigital Hyperplasia 111
Double sole + White line separation 110
Cork screw claw 102
Youngstock survival 101

NAV proof run date: 04-11-2025 Reliability 80 % Number of daughters: 0

Functional

Trait Index 80 100 120
Milkability 111
Temperament 99

NAV proof run date: 04-11-2025 Reliability 61 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 118
Stature 119 Short Tall
Body depth 106 Shallow Deep
Chest width 104 Narrow Wide
Rib structure 110 Coarse Angular
Top line 98 Weak Strong
Rump width 115 Narrow pins Wide pins
Rump angle 97 High pins Low pins
Feet & legs 98
Rear legs, side view 101 Straight Sickled
Rear legs, back rear view 108 Toes out Parallel, bow-legged
Foot angle 95 Low Steep
Bone quality 94 Coarse Fine and thin
Hock quality 93 Filled Dry
Udder 113
Fore udder attachment 113 Loose Strong
Rear udder height 117 Low High
Rear udder width 122 Narrow Wide
Udder support 100 Weak Strong
Udder depth 115 Deep High
Udder balance 122 Deep rear udder Deep front udder
Teat length 105 Short Long
Teat thickness 105 Thin Thick
Teat placement (front) 99 Wide Close
Teat placement (back) 103 Wide Close

NAV proof run date: 04-11-2025 Reliability 61 % 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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