Fgfr1op2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fgfr1op2
FGFR1 oncogene partner 2
MGI:1914779

17 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Fgfr1op2^em1(IMPC)Mbp/Fgfr1op2⁺ C57BL/6N-Fgfr1op2^em1(IMPC)Mbp/MbpMmucd	abnormal placenta morphology	J:211773
	abnormal retina morphology	J:211773
	abnormal skin morphology	J:211773
	abnormal vitreous body morphology	J:211773
	cataract	J:211773
	microphthalmia	J:211773
	persistence of hyaloid vascular system	J:211773
Fgfr1op2^em1(IMPC)Mbp/Fgfr1op2^em1(IMPC)Mbp C57BL/6N-Fgfr1op2^em1(IMPC)Mbp/MbpMmucd	abnormal blood vessel morphology	J:211773
	abnormal craniofacial morphology	J:211773
	abnormal limb morphology	J:211773
	abnormal placenta morphology	J:211773
	abnormal placenta size	J:211773
	abnormal placenta vasculature	J:211773
	abnormal tail morphology	J:211773
	cleft palate	J:211773
	edema	J:211773
	embryonic growth retardation	J:211773
	preweaning lethality, complete penetrance	J:211773

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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