Fgf22 Phenotype Annotations

About Help FAQ

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fgf22
fibroblast growth factor 22
MGI:1914362

11 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fgf22^{tm1b(EUCOMM)Hmgu}/Fgf22^{tm1b(EUCOMM)Hmgu} C57BL/6N-Fgf22^{tm1b(EUCOMM)Hmgu}/H	abnormal gait	J:211773
	increased circulating amylase level	J:211773
Fgf22^tm1Dgen/Fgf22^tm1Dgen B6.Cg-Fgf22^tm1Dgen	decreased susceptibility to pharmacologically induced seizures	J:161954
Fgf22^tm1Dgen/Fgf22^tm1Dgen Not Specified	abnormal synaptic vesicle clustering	J:161954
	abnormal synaptic vesicle morphology	J:161954
	abnormal synaptic vesicle number	J:161954
	decreased miniature excitatory postsynaptic current frequency	J:161954
	enhanced paired-pulse facilitation	J:161954
	increased synaptic depression	J:161954
Fgf22^tm1Rpgr/Fgf22^tm1Rpgr involves: 129P2/OlaHsd * C57BL/6	decreased incidence of tumors by chemical induction	J:187809
	normal integument phenotype	J:187809

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23