VH Bertram - DEU 362802979

Production & Efficiency

Trait Index 80 100 120
Production 114
Milk kg 109
Fat, kg 115
Fat, % 104
Protein kg 112
Protein % 102
Persistency 88
Growth 87
Daily carcass gain 84
Carcass conformation score 93
Saved feed 94
Maintenance efficiency 107

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 8035

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 109 295.3 11758
Fat kg, 305 days 115 18.7 487
Fat %, 305 days 104 0.06 4.2
Protein kg, 305 days 112 12.0 416
Protein %, 305 days 102 0.01 3.6

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 8035

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 104
Interval from calving to first insemination (cows) 102
Interval from first to last insemination (heifers) 100
Interval from first to last insemination (cows) 105
Number of inseminations (heifers) 99
Number of inseminations (cows) 103
Calving sire 95
Calving maternal 107
Udder health 104
General health 105
Longevity 106
Hoof health 97
Sole Ulcer 100
Sole Hemorrhage 93
Heel Horn Erosion 101
Digital dermatitis + Interdigital Dermatitis 91
Verrucose dermatitis + Interdigital Hyperplasia 98
Double sole + White line separation 92
Cork screw claw 111
Youngstock survival 89

NAV proof run date: 05-05-2026 Reliability 99 % Number of daughters: 6422

Functional

Trait Index 80 100 120
Milkability 110
Temperament 112

NAV proof run date: 05-05-2026 Reliability 97 % Number of daughters: 3158

Conformation

Trait Index 80 100 120
Frame 99
Stature 98 Short Tall
Body depth 98 Shallow Deep
Chest width 97 Narrow Wide
Rib structure 112 Coarse Angular
Top line 100 Weak Strong
Rump width 94 Narrow pins Wide pins
Rump angle 87 High pins Low pins
Feet & legs 105
Rear legs, side view 95 Straight Sickled
Rear legs, back rear view 98 Toes out Parallel, bow-legged
Foot angle 112 Low Steep
Bone quality 108 Coarse Fine and thin
Hock quality 101 Filled Dry
Udder 111
Fore udder attachment 113 Loose Strong
Rear udder height 116 Low High
Rear udder width 112 Narrow Wide
Udder support 108 Weak Strong
Udder depth 105 Deep High
Udder balance 96 Deep rear udder Deep front udder
Teat length 95 Short Long
Teat thickness 93 Thin Thick
Teat placement (front) 97 Wide Close
Teat placement (back) 105 Wide Close

NAV proof run date: 05-05-2026 Reliability 97 % Number of daughters: 3158

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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