Name ID |
FVB.129-Mn1tm1Ecz MGI:3581844 |
Darker colors indicate more annotations |
Mouse Phenotypes | abnormal cranial suture morphology |
abnormal frontal bone morphology |
abnormal interparietal bone morphology |
abnormal parietal bone morphology |
abnormal pterygoid process morphology |
abnormal sphenoid bone morphology |
abnormal supraoccipital bone morphology |
absent alisphenoid bone |
absent temporal bone squamous part |
absent vomer bone |
alisphenoid bone hypoplasia |
basisphenoid bone hypoplasia |
cleft secondary palate |
large cranial foramen ovale |
large foramen rotundum |
maxillary shelf hypoplasia |
palatal shelves fail to meet at midline |
palate bone hypoplasia |
palatine bone horizontal plate hypoplasia |
presphenoid bone hypoplasia |
pterygoid bone hypoplasia |
temporal bone hypoplasia |
thin frontal bone |
thin interparietal bone |
thin parietal bone |
vomer bone hypoplasia |
|
Availability | Mouse Genotype | ||||||||||||||||||||||||||
Mn1tm1Ecz/Mn1+ | |||||||||||||||||||||||||||
Mn1tm1Ecz/Mn1tm1Ecz |