Prrc2b Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Prrc2b
proline-rich coiled-coil 2B
MGI:1923304

28 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Prrc2b^{tm1a(EUCOMM)Wtsi}/Prrc2b^{tm1a(EUCOMM)Wtsi} C57BL/6N-Prrc2b^{tm1a(EUCOMM)Wtsi}/Wtsi	abnormal eye morphology	J:239583
	abnormal eye muscle morphology	J:239583
	abnormal forebrain morphology	J:239583
	abnormal hypoglossal nerve topology	J:239583
	abnormal optic cup morphology	J:239583
	abnormal pulmonary valve cusp morphology	J:239583
	abnormal skeletal muscle morphology	J:239583
	abnormal thyroid gland morphology	J:239583
	abnormal vitelline vein topology	J:239583
	absent hypoglossal canal	J:239583
	absent hypoglossal nerve	J:239583
	absent segment of posterior cerebral artery	J:239583
	absent skeletal muscle	J:239583
	arteriovenous malformation	J:239583
	dilated liver sinusoidal space	J:239583
	dilated vasculature	J:239583
	eye hemorrhage	J:239583
	fusion of vertebral arches	J:239583
	hemorrhage	J:239583
	left sided brachiocephalic trunk	J:239583
	lens vacuoles	J:239583
	perimembraneous ventricular septal defect	J:239583
	persistent right 6th pharyngeal arch artery	J:239583
	persistent right dorsal aorta	J:239583
	persistent trigeminal artery	J:239583
	preweaning lethality, complete penetrance	J:211773
	retropleural edema	J:239583
	right aortic arch	J:239583

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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