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

Narrow internal auditory canal

Chronic otitis media

Conductive hearing impairment

Mixed hearing impairment

Atresia of the external auditory canal

Stenosis of the external auditory canal

Abnormal pinna morphology

Abnormal antihelix morphology

Prominent crus of helix

Low-set ears

Posteriorly rotated ears

Microtia

Cupped ear

Sensorineural hearing impairment

Hearing impairment

Disease(s) Associated with FGFR2

acrocephalosyndactylia

Antley-Bixler syndrome without disordered steroidogenesis

Beare-Stevenson cutis gyrata syndrome

craniosynostosis

Crouzon syndrome

lacrimoauriculodentodigital syndrome 1

Saethre-Chotzen syndrome

Mouse Phenotypes

inner ear cyst

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

Availability

Mouse Genotype

Fgfr2^m1Sgg/Fgfr2^m1Sgg

Fgfr2^tm1.1Dsn/Fgfr2^tm1.1Dsn

Fgfr2^tm1Cxd/Fgfr2^tm1Cxd

Fgfr2^tm3Dsn/Fgfr2^tm3Dsn

Fgfr2^m1Sgg/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)
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