VR Vehmaa - FIN 48510

Production & Efficiency

Trait Index 80 100 120
Production 116
Milk kg 102
Fat, kg 119
Fat, % 121
Protein kg 108
Protein % 110
Persistency 111
Growth 99
Daily carcass gain 100
Carcass conformation score 99
Saved feed 90
Maintenance efficiency 90
Metabolic efficiency 100

NAV proof run date: 03-10-2023 Reliability 81 % Number of daughters: 0

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 102 69.9 9792
Fat kg, 305 days 119 25.7 433
Fat %, 305 days 121 0.27 4.5
Protein kg, 305 days 108 8.5 354
Protein %, 305 days 110 0.07 3.6

NAV proof run date: 03-10-2023 Reliability 81 % Number of daughters: 0

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 105
Interval from calving to first insemination (cows) 102
Interval from first to last insemination (cows) 106
Calving sire 106
Calving maternal 104
Udder health 111
General health 102
Longevity 109
Hoof health 102
Sole Ulcer 93
Sole Hemorrhage 104
Heel Horn Erosion 106
Digital dermatitis + Interdigital Dermatitis 104
Verrucose dermatitis + Interdigital Hyperplasia 102
Double sole + White line separation 78
Cork screw claw 95
Youngstock survival 117

NAV proof run date: 03-10-2023 Reliability 75 % Number of daughters: 0

Functional

Trait Index 80 100 120
Milkability 104
Temperament 107

NAV proof run date: 03-10-2023 Reliability 55 % Number of daughters: 0

Conformation

Trait Index 80 100 120
Frame 119
Stature 108 Short Tall
Body depth 117 Shallow Deep
Chest width 116 Narrow Wide
Dairy form 108 Coarse Angular
Top line 88 Weak Strong
Rump width 108 Narrow pins Wide pins
Rump angle 88 High pins Low pins
Feet & legs 99
Rear legs, side view 93 Straight Sickled
Rear legs, back rear view 102 Toes out Parallel, bow-legged
Foot angle 103 Low Steep
Bone quality 99 Coarse Fine and thin
Hock quality 95 Filled Dry
Udder 111
Fore udder attachment 117 Loose Strong
Rear udder height 110 Low High
Rear udder width 107 Narrow Wide
Udder support 100 Weak Strong
Udder depth 107 Deep High
Udder balance 108 Deep rear udder Deep front udder
Teat length 99 Short Long
Teat thickness 101 Thin Thick
Teat placement (front) 102 Wide Close
Teat placement (back) 99 Wide Close

NAV proof run date: 03-10-2023 Reliability 55 % Number of daughters: 0

Monogenic

Name Scientific name Symptoms Code Result
SPAST Bovine Spinal Dysmyelination (SDF = Not carrier, SDC = Single carrier, SDS = Double carrier) Spinal dysmyelination is a Read more (SDF = Not carrier, SDC = Single carrier, SDS = Double carrier) Spinal dysmyelination is a recessive congenital neurodegenerative defect identified in the Brown Swiss population. It is a disorder in the central nervous system and is caused by a defect in the neuronal pathways. Affected calves are unable to stand due to spasms of the limbs and the body. The calves die shortly after birth. The key ancestor is believed to be White Cloud Jason’s Elegant (US 148551). https://omia.org/OMIA001247/9913/ SDF Free
SMA Spinal muscular atrophy (SMF = Not carrier, SMC = Single carrier, SMS = Double carrier) Spinal muscular atrophy is Read more (SMF = Not carrier, SMC = Single carrier, SMS = Double carrier) Spinal muscular atrophy is an autosomal recessively inherited defect in the Brown Swiss population. It is a neuromuscular disorder characterised by a loss of lower motor neurons and progressive muscle wasting. The nerve cells in the spinal cord that control muscle function die, which causes muscle wastage. It is most frequently seen in 1-12 weeks old calves, but in some cases, it can be seen from birth. It causes the calves to become weak and have problems standing, the symptoms progressively worsen until the calves die or are euthanized. The key ancestor is the Brown Swiss bull Meadow View Destiny (US 118619). https://omia.org/OMIA000939/9913/ SMF Free
BTA12 Bos Taurus Autosome 12 (B12F = Not carrier, B12C = Single carrier, B12S = Double carrier) BTA12 is an Read more (B12F = Not carrier, B12C = Single carrier, B12S = Double carrier) BTA12 is an autosomal recessively inherited disease, in the Nordic Red Dairy Cattle population. It causes early embryonic death (spontaneous abortion), between the first and fifth month of gestation. The mutation occurs in the RNASEH2B gene. https://omia.org/OMIA001901/9913/ B12F Free
BTA23 Bos Taurus Autosome 23 (B23F = Not carrier, B23C = Single carrier, B23S = Double carrier) BTA23 is an autosomal Read more (B23F = Not carrier, B23C = Single carrier, B23S = Double carrier) BTA23 is an autosomal recessively inherited defect. The disorder was identified in the Nordic Red Dairy Cattle population and causes embryonic death (spontaneous abortion), late in gestation or stillborn calves. The calves have no deformities. B23F Free
PIRM Ptosis, intellectual disability, retarded growth and mortality (PIF = Not carrier, PIC = Single carrier, PIS = Double carrier) AH1 is an autosomal Read more (PIF = Not carrier, PIC = Single carrier, PIS = Double carrier) AH1 is an autosomal recessively inherited defect, identified in the Canadian and Nordic Ayrshire populations. AH1 and PIRM are located very closely to each other in the genome, and it is expected that they are the same defect. They primarily cause early embryonic death (spontaneous abortion) within the first 100 days of gestation. If affected calves are born, they are malformed and have inhibited growth. There has also been reports of learning disabilities (e.g. difficulties learning to drink) The key ancestor is believed to be Selwood Betty’s Commander (CAN 393145). https://omia.org/OMIA001934/9913/ PIF Free
BH2 Braunvieh Haplotype 2 Many of the calves with the mutation in double dose (homozygotic) are stillborn or die Read more Many of the calves with the mutation in double dose (homozygotic) are stillborn or die shortly after birth. It is common for them that they have a low birth weight and are underdeveloped. The calves, which live longer, suffer from chronic lung defect resulting in little growth and high young animal mortality. Most of these calves die or are put down within the first month, however a few can survive. Surviving calves suffer from repeated airway defects and inhibitory growth, and will most likely die or be put down BH2F Free
AH2 Ayrshire Haplotype 2 (AH2F = Not carrier, AH2C = Single carrier, AH2S = Double carrier) AH2 is an autosomal Read more (AH2F = Not carrier, AH2C = Single carrier, AH2S = Double carrier) AH2 is an autosomal recessively inherited defect, identified in the North American Ayrshire population. It causes early embryonic death (spontaneous abortion). The key ancestor is believed to be Oak-Ridge Lightning (US 120135). https://omia.org/OMIA002134/9913/ AH2F Free

Want to know more?
Send us a message.

Name

Country

Phone

Post code

Your message