VH Bayline - DEU 363894948

Production & Efficiency

Trait Index 80 100 120
Production 120
Milk kg 119
Fat, kg 120
Fat, % 100
Protein kg 120
Protein % 99
Persistency 106
Growth 115
Daily carcass gain 125
Carcass conformation score 101
Saved feed 82
Maintenance efficiency 89
Metabolic efficiency 93

NAV proof run date: 05-11-2024 Reliability 77 % Number of daughters: 0

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 119 623.3 11488
Fat kg, 305 days 120 25.0 470
Fat %, 305 days 100 0.00 4.1
Protein kg, 305 days 120 20.0 402
Protein %, 305 days 99 -0.01 3.5

NAV proof run date: 05-11-2024 Reliability 77 % Number of daughters: 0

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 102
Interval from calving to first insemination (cows) 95
Interval from first to last insemination (heifers) 100
Interval from first to last insemination (cows) 103
Number of inseminations (heifers) 100
Number of inseminations (cows) 102
Calving sire 95
Calving maternal 109
Udder health 98
General health 107
Longevity 111
Hoof health 99
Sole Ulcer 93
Sole Hemorrhage 99
Heel Horn Erosion 116
Digital dermatitis + Interdigital Dermatitis 104
Verrucose dermatitis + Interdigital Hyperplasia 103
Double sole + White line separation 97
Cork screw claw 115
Youngstock survival 96

NAV proof run date: 05-11-2024 Reliability 76 % Number of daughters: 0

Functional

Trait Index 80 100 120
Milkability 101
Temperament 112

NAV proof run date: 05-11-2024 Reliability 55 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 118
Stature 113 Short Tall
Body depth 103 Shallow Deep
Chest width 115 Narrow Wide
Rib structure 111 Coarse Angular
Top line 108 Weak Strong
Rump width 116 Narrow pins Wide pins
Rump angle 94 High pins Low pins
Feet & legs 110
Rear legs, side view 104 Straight Sickled
Rear legs, back rear view 112 Toes out Parallel, bow-legged
Foot angle 104 Low Steep
Bone quality 104 Coarse Fine and thin
Hock quality 102 Filled Dry
Udder 111
Fore udder attachment 100 Loose Strong
Rear udder height 120 Low High
Rear udder width 126 Narrow Wide
Udder support 104 Weak Strong
Udder depth 107 Deep High
Udder balance 109 Deep rear udder Deep front udder
Teat length 103 Short Long
Teat thickness 97 Thin Thick
Teat placement (front) 98 Wide Close
Teat placement (back) 95 Wide Close

NAV proof run date: 05-11-2024 Reliability 55 % 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

Want to know more?
Send us a message.

Name

Country

Phone

Post code

Your message