About   Help   FAQ
Symbol
Name
ID
Fgfr2
fibroblast growth factor receptor 2
MGI:95523
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Sensorineural hearing impairment
Mixed hearing impairment
Narrow internal auditory canal
Conductive hearing impairment
Chronic otitis media
Low-set ears
Low-set, posteriorly rotated ears
Prominent crus of helix
Atresia of the external auditory canal
Stenosis of the external auditory canal
Abnormality of the pinna
Abnormality of the antihelix
Cupped ear
Microtia
External ear malformation
Hearing impairment
Disease(s) Associated with FGFR2
acrocephalosyndactylia
Antley-Bixler syndrome
Beare-Stevenson cutis gyrata syndrome
Crouzon syndrome
LADD syndrome
pre-eclampsia
Saethre-Chotzen syndrome

Mouse Phenotypes
abnormal ear development
abnormal otic vesicle development
small otic vesicle
abnormal cochlea morphology
abnormal cochlear sensory epithelium morphology
abnormal semicircular canal morphology
abnormal membranous labyrinth morphology
abnormal endolymphatic duct morphology
abnormal otic capsule morphology
small otic capsule
inner ear cysts
Availability Mouse Genotype
Fgfr2m1Sgg/Fgfr2m1Sgg
Fgfr2tm1.1Dsn/Fgfr2tm1.1Dsn
Fgfr2tm1Cxd/Fgfr2tm1Cxd
Fgfr2tm3Dsn/Fgfr2tm3Dsn
Fgfr2m1Sgg/Fgfr2+

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 & Copyright Notice
Send questions and comments to User Support.
last database update
11/05/2019
MGI 6.14
The Jackson Laboratory