Pcdha9 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Pcdha9
protocadherin alpha 9
MGI:2447322

22 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pcdha9^b2b635.1Clo/Pcdha9^b2b635.1Clo C57BL/6J-Pcdha9^b2b635.1Clo	aorta hypoplasia	J:242757
	aorta stenosis	J:242757
	bicuspid aortic valve	J:242757
	cardiac hypertrophy	J:242757
Pcdha9^em1Zhxu/Pcdha9⁺ C57BL/6-Pcdha9^em1Zhxu	impaired coordination	J:360856
Pcdha9^em1Zhxu/Pcdha9⁺ C57BL/6-Pcdha9^em1Zhxu	impaired limb coordination	J:360856
Pcdha9^em1Zhxu/Pcdha9^em1Zhxu C57BL/6-Pcdha9^em1Zhxu	abnormal gait	J:360856
	abnormal motor capabilities/coordination/movement	J:360856
	abnormal muscle electrophysiology	J:360856
	abnormal neuromuscular synapse morphology	J:360856
	abnormal sciatic nerve morphology	J:360856
	abnormal synaptic bouton morphology	J:360856
	astrocytosis	J:360856
	decreased grip strength	J:360856
	hemiplegia	J:360856
	impaired coordination	J:360856
	impaired limb coordination	J:360856
	kyphosis	J:360856
	motor neuron degeneration	J:360856
	muscular atrophy	J:360856
	neuronal cytoplasmic inclusions	J:360856
	premature death	J:360856
	short stride length	J:360856
	weight loss	J:360856
Pcdha9^em2Zhxu/Pcdha9^em2Zhxu C57BL/6-Pcdha9^em2Zhxu	abnormal gait	J:360856
	abnormal motor capabilities/coordination/movement	J:360856
	abnormal neuromuscular synapse morphology	J:360856
	abnormal synaptic bouton morphology	J:360856
	decreased grip strength	J:360856
	hemiplegia	J:360856
	impaired coordination	J:360856
	impaired limb coordination	J:360856
	kyphosis	J:360856
	muscular atrophy	J:360856
	premature death	J:360856
	short stride length	J:360856
	weight loss	J:360856

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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