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Symbol
Name
ID

Tfap2a
transcription factor AP-2, alpha
MGI:104671

Phenotype annotations related to hearing/vestibular/ear

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Fusion of middle ear ossicles	Conductive hearing impairment	Overfolded helix	Hypoplastic superior helix	Low-set ears	Posteriorly rotated ears	Microtia	Sensorineural hearing impairment	Hearing impairment
Disease(s) Associated with TFAP2A
branchiooculofacial syndrome

Mouse Phenotypes		hearing/vestibular/ear phenotype	abnormal middle ear ossicle morphology	abnormal incus morphology	abnormal malleus morphology	abnormal stapes morphology	absent middle ear ossicles	absent outer ear	absent tympanic ring	decreased cochlear nerve compound action potential	conductive hearing loss
Availability	Mouse Genotype	hearing/vestibular/ear phenotype	abnormal middle ear ossicle morphology	abnormal incus morphology	abnormal malleus morphology	abnormal stapes morphology	absent middle ear ossicles	absent outer ear	absent tympanic ring	decreased cochlear nerve compound action potential	conductive hearing loss
	Tfap2a^tm1Jae/Tfap2a^tm1Jae
	Tfap2a^tm1Will/Tfap2a^tm1Will
	Tfap2a^Mhdador/Tfap2a⁺
	Tfap2a^tm1Jae/Tfap2a⁺
	Tfap2a^tm1Will/Tfap2a⁺	*
	Tfap2a^tm1Hsv/Tfap2a^tm2Will H2az2^{Tg(Wnt1-cre)11Rth}/H2az2⁺ (conditional)

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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