|
|
 |
| SILVERRIDGE V EINSTEIN |
 |
| CLAYNOOK ZIVA HOUSE VG-86-2YR-CAN 3* |
|
|
 |
 |
| LEANINGHOUSE HELIX 22137 |
 |
| MORNINGVIEW DUKE ZIP GP-84-2YR-CAN 21* |
|
|
 |
 |
| S-S-I MONTROSS DUKE |
 |
| MORNINGVIEW YODER ZEPLIN EX-90-2E-USA DOM |
|
|
|
| TD TR TL TY MWT TV 99%-I |
HH1F HH2F HH3F HH4F HH5F HH6F HCDF HMWF |
| Reg. #: HOCANM13601249 |
aAa: 432516 |
DMS: 123,135 |
| Born: 06/18/2020 |
Kappa Casein: AB |
Beta Casein: A2A2 |
|
| SEMEX MANAGEMENT TRAITS |
|
 |
| Immunity |
97 |
 |
Calf Immunity |
91 |
 |
Robot Index |
98 |
|
| PRODUCTION |
| 105 Herds |
548 Dtrs |
92% Rel |
|
MACE-G / 08-26 |
|
 |
Milk lbs 551 |
 |
Fat lbs 75 |
 |
Fat % +0.19 |
 |
Protein lbs 33 |
 |
Protein % +0.06 |
 |
| NM$ 389 |
 |
CM$ 415 |
 |
FM$ 330 |
 |
GM$ 382 |
 |
DWP$ 493 |
 |
Feed Efficiency 138 |
 |
RFI 226 |
 |
Feed Saved -442 |
 |
Methane Efficiency 107 |
 |
Milking Speed 7.15 |
 |
|
Daughter Average (ME)
Milk 27,242 lbs
Fat 1,233 lbs
Protein 928 lbs
|
|
 |
|
 |
|
 |
|
 |
| Heifer Conception Rate | 0.9 | |
|
 |
| Daughter Pregnancy Rate | 0.7 |
|
 |
| Sire Calving Ease | 1.8% | 74% Rel |
|
 |
|
 |
| Daughter Calving Ease | 2.2% | 72% Rel |
|
 |
|
 |
|
 |
|
 |
|
 |
 |
|
| CONFORMATION |
| 29 Herds |
132 Dtrs |
88% Rel |
|
MACE-G / 08-26 |
|
|
 |
| HO Conformation Composite | 0.28 | |
|
 |
|
 |
|
 |
| Feet & Legs Composite | -0.04 |
|
 |
|
 |
 |
|
|
|
| Stature |
|
|
Tall |
+1.29 |
| Strength |
|
|
Strong |
+1.36 |
| Body Depth |
|
|
Deep |
+1.30 |
| Dairy Form |
|
|
Open Rib |
+0.81 |
| Rump Angle |
|
|
High |
-0.13 |
| Rump Width |
|
|
Wide |
+1.93 |
| Rear Legs Side View |
|
|
Posty |
-0.85 |
| Rear Legs Rear View |
|
|
Hock-in |
-0.31 |
| Foot Angle |
|
|
Steep |
+0.78 |
| F & L Score |
|
|
High |
+0.38 |
| Fore Attachment |
|
|
Strong |
+1.79 |
| Rear Udder Height |
|
|
High |
+1.59 |
| Rear Udder Width |
|
|
Wide |
+2.93 |
| Udder Cleft |
|
|
Strong |
+2.35 |
| Udder Depth |
|
|
Shallow |
+1.13 |
| Fore Teat Placement |
|
|
Close |
+2.06 |
| Teat Length |
|
|
Short |
-0.56 |
| Rear Teat Placement |
|
|
Close |
+2.36 |
|
|
|
| |
|
|
|
|