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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
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Allelic Composition
Genetic Background		 Annotated Term Reference
Fgfr1op2em1(IMPC)Mbp/Fgfr1op2+
C57BL/6N-Fgfr1op2em1(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
Fgfr1op2em1(IMPC)Mbp/Fgfr1op2em1(IMPC)Mbp
C57BL/6N-Fgfr1op2em1(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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Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory