VH Bayline - DEU 363894948

Production & Efficiency

Trait Index 80 100 120
Production 117
Milk kg 121
Fat, kg 117
Fat, % 96
Protein kg 118
Protein % 92
Persistency 105
Growth 120
Daily carcass gain 125
Carcass conformation score 108
Saved feed 100
Maintenance efficiency 89

NAV proof run date: 01-09-2026 Reliability 94 % Number of daughters: 50

Expected Progeny Difference

Trait Index Bull effect Average
Milk lbs, 305 days 121 1,518.76 25,921.95
Fat lbs, 305 days 117 46.74 1,073.65
Fat %, 305 days 96 -0.06 4.2
Protein lbs, 305 days 118 39.68 917.12
Protein %, 305 days 92 -0.06 3.6

NAV proof run date: 01-09-2026 Reliability 94 % Number of daughters: 50

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 103
Interval from calving to first insemination (cows) 94
Interval from first to last insemination (heifers) 109
Interval from first to last insemination (cows) 103
Number of inseminations (heifers) 110
Number of inseminations (cows) 104
Calving sire 95
Calving maternal 106
Udder health 100
General health 110
Longevity 109
Hoof health 101
Sole Ulcer 97
Sole Hemorrhage 101
Heel Horn Erosion 116
Digital dermatitis + Interdigital Dermatitis 97
Verrucose dermatitis + Interdigital Hyperplasia 102
Double sole + White line separation 95
Cork screw claw 117
Youngstock survival 94

NAV proof run date: 01-09-2026 Reliability 86 % Number of daughters: 23

Functional

Trait Index 80 100 120
Milkability 106
Temperament 118

NAV proof run date: 01-09-2026 Reliability 66 % Number of daughters: 5

Conformation

Trait Index 80 100 120
Frame 121
Stature 115 Short Tall
Body depth 104 Shallow Deep
Chest width 119 Narrow Wide
Rib structure 106 Coarse Angular
Top line 109 Weak Strong
Rump width 121 Narrow pins Wide pins
Rump angle 93 High pins Low pins
Feet & legs 108
Rear legs, side view 103 Straight Sickled
Rear legs, back rear view 110 Toes out Parallel, bow-legged
Foot angle 105 Low Steep
Bone quality 101 Coarse Fine and thin
Hock quality 102 Filled Dry
Udder 113
Fore udder attachment 101 Loose Strong
Rear udder height 116 Low High
Rear udder width 127 Narrow Wide
Udder support 103 Weak Strong
Udder depth 108 Deep High
Udder balance 104 Deep rear udder Deep front udder
Teat length 102 Short Long
Teat thickness 94 Thin Thick
Teat placement (front) 99 Wide Close
Teat placement (back) 93 Wide Close

NAV proof run date: 01-09-2026 Reliability 66 % Number of daughters: 5

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