|
|
 |
| PROGENESIS MAESTRO |
 |
| CLAYNOOK FLOTILLA TOPNOTCH EX-91-2E-CAN |
|
|
 |
 |
| PROGENESIS TOPNOTCH |
 |
| CLAYNOOK FRANCIS DUKE VG-85-2YR-CAN 2* |
|
|
 |
 |
| S-S-I MONTROSS DUKE |
 |
| CLAYNOOK FLOUNDER SILVER VG-85-2YR-CAN |
|
|
|
| TD TR TL TY MWT TV 99%-I |
HH1F HH2F HH3F HH4F HH5F HH6F HCDF HMWF |
| Reg. #: HOCANM13601229 |
aAa: 243561 |
DMS: 135,345 |
| Born: 03/16/2020 |
Kappa Casein: AA |
Beta Casein: A1A1 |
|
| SEMEX MANAGEMENT TRAITS |
|
 |
| Immunity |
103 |
 |
Calf Immunity |
96 |
 |
Robot Index |
102 |
|
| PRODUCTION |
| 243 Herds |
2013 Dtrs |
99% Rel |
|
MACE-G / 08-26 |
|
 |
Milk lbs 1165 |
 |
Fat lbs 33 |
 |
Fat % -0.06 |
 |
Protein lbs 42 |
 |
Protein % +0.01 |
 |
| NM$ 563 |
 |
CM$ 578 |
 |
FM$ 531 |
 |
GM$ 580 |
 |
DWP$ 468 |
 |
Feed Efficiency 142 |
 |
RFI -156 |
 |
Feed Saved 81 |
 |
Methane Efficiency 96 |
 |
Milking Speed 7.03 |
 |
|
Daughter Average (ME)
Milk 27,531 lbs
Fat 1,126 lbs
Protein 920 lbs
|
|
 |
|
 |
|
 |
|
 |
| Heifer Conception Rate | 1.4 | |
|
 |
| Daughter Pregnancy Rate | 1.9 |
|
 |
| Sire Calving Ease | 1.6% | 94% Rel |
|
 |
|
 |
| Daughter Calving Ease | 1.9% | 88% Rel |
|
 |
|
 |
|
 |
|
 |
|
 |
 |
|
| CONFORMATION |
| 99 Herds |
567 Dtrs |
97% Rel |
|
MACE-G / 08-26 |
|
|
 |
| HO Conformation Composite | 1.67 | |
|
 |
|
 |
|
 |
| Feet & Legs Composite | 0.89 |
|
 |
|
 |
 |
|
|
|
| Stature |
|
|
Tall |
+0.70 |
| Strength |
|
|
Strong |
+0.31 |
| Body Depth |
|
|
Deep |
+0.26 |
| Dairy Form |
|
|
Open Rib |
+0.39 |
| Rump Angle |
|
|
Sloped |
+1.07 |
| Rump Width |
|
|
Wide |
+1.41 |
| Rear Legs Side View |
|
|
Posty |
-0.46 |
| Rear Legs Rear View |
|
|
Straight |
+0.64 |
| Foot Angle |
|
|
Steep |
+1.04 |
| F & L Score |
|
|
High |
+1.07 |
| Fore Attachment |
|
|
Strong |
+0.79 |
| Rear Udder Height |
|
|
High |
+1.62 |
| Rear Udder Width |
|
|
Wide |
+1.51 |
| Udder Cleft |
|
|
Strong |
+1.57 |
| Udder Depth |
|
|
Shallow |
+1.08 |
| Fore Teat Placement |
|
|
Close |
+0.99 |
| Teat Length |
|
|
Short |
-0.27 |
| Rear Teat Placement |
|
|
Close |
+1.67 |
|
|
|
| |
|
|
|
|