VH Mulan P - DNK 262801 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 113
Milk kg 112
Fat, kg 114
Fat, % 101
Protein kg 112
Protein % 98
Persistency 101
Growth 109
Daily carcass gain 126
Carcass conformation score 92
Saved feed 97
Maintenance efficiency 88

NAV proof run date: 06-10-2026 Reliability 92 % Number of daughters: 16

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 112 393.7 11758
Fat kg, 305 days 114 17.5 487
Fat %, 305 days 101 0.02 4.2
Protein kg, 305 days 112 12.0 416
Protein %, 305 days 98 -0.01 3.6

NAV proof run date: 06-10-2026 Reliability 92 % Number of daughters: 16

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 93
Interval from calving to first insemination (cows) 85
Interval from first to last insemination (heifers) 89
Interval from first to last insemination (cows) 95
Number of inseminations (heifers) 99
Number of inseminations (cows) 99
Calving sire 107
Calving maternal 102
Udder health 98
General health 94
Longevity 109
Hoof health 100
Sole Ulcer 99
Sole Hemorrhage 95
Heel Horn Erosion 98
Digital dermatitis + Interdigital Dermatitis 104
Verrucose dermatitis + Interdigital Hyperplasia 104
Double sole + White line separation 106
Cork screw claw 99
Youngstock survival 106

NAV proof run date: 06-10-2026 Reliability 82 % Number of daughters: 8

Functional

Trait Index 80 100 120
Milkability 112
Temperament 99

NAV proof run date: 06-10-2026 Reliability 65 % Number of daughters: 8

Conformation

Trait Index 80 100 120
Frame 115
Stature 117 Short Tall
Body depth 106 Shallow Deep
Chest width 104 Narrow Wide
Rib structure 106 Coarse Angular
Top line 97 Weak Strong
Rump width 114 Narrow pins Wide pins
Rump angle 94 High pins Low pins
Feet & legs 99
Rear legs, side view 101 Straight Sickled
Rear legs, back rear view 110 Toes out Parallel, bow-legged
Foot angle 93 Low Steep
Bone quality 97 Coarse Fine and thin
Hock quality 92 Filled Dry
Udder 113
Fore udder attachment 114 Loose Strong
Rear udder height 119 Low High
Rear udder width 123 Narrow Wide
Udder support 101 Weak Strong
Udder depth 117 Deep High
Udder balance 127 Deep rear udder Deep front udder
Teat length 106 Short Long
Teat thickness 106 Thin Thick
Teat placement (front) 97 Wide Close
Teat placement (back) 103 Wide Close

NAV proof run date: 06-10-2026 Reliability 65 % Number of daughters: 8

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