37 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Man2b1tm1Psa/Man2b1tm1Psa involves: 129 * C57BL/6J	abnormal axon morphology	J:56659, J:99812
	abnormal brainstem morphology	J:56659, J:99812
	abnormal cerebral cortex morphology	J:56659, J:99812
	abnormal cochlea morphology	J:99812
	abnormal cochlear ganglion morphology	J:99812
	abnormal cornea endothelium morphology	J:56659
	abnormal cornea stroma morphology	J:56659
	abnormal cranial ganglia morphology	J:99812
	abnormal eye morphology	J:56659
	abnormal eye muscle morphology	J:56659
	abnormal forebrain morphology	J:99812
	abnormal glial cell morphology	J:99812
	abnormal globus pallidus morphology	J:99812
	abnormal hepatocyte morphology	J:56659
	abnormal hippocampus CA2 region morphology	J:99812
	abnormal hippocampus CA3 region morphology	J:99812
	abnormal hippocampus morphology	J:99812
	abnormal homeostasis	J:56659
	abnormal Kupffer cell morphology	J:56659
	abnormal liver morphology	J:56659
	abnormal lysosome morphology	J:56659, J:99812
	abnormal neuron morphology	J:56659, J:99812
	abnormal olfactory discrimination memory	J:99812
	abnormal pancreatic acinar cell morphology	J:56659
	abnormal passive avoidance behavior	J:99812
	abnormal renal tubule epithelium morphology	J:56659
	abnormal retina photoreceptor morphology	J:56659
	abnormal skeleton morphology	J:56659
	abnormal spatial learning	J:99812
	abnormal spiral ligament fibrocyte morphology	J:99812
	abnormal spleen red pulp morphology	J:56659
	abnormal trigeminal ganglion morphology	J:99812
	abnormal urine homeostasis	J:56659
	abnormal vestibular ganglion morphology	J:99812
	decreased body weight	J:99812
	decreased exploration in new environment	J:99812
	enhanced long-term potentiation	J:99812