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Symbol
Name
ID

Tfap2b
transcription factor AP-2 beta
MGI:104672

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Intellectual disability, mild	Parasomnia	Global developmental delay
Disease(s) Associated with TFAP2B
Char syndrome

Mouse Phenotypes		gliosis	decreased amacrine cell number	retina ganglion cell degeneration	abnormal optic disk morphology	optic nerve cupping	optic nerve degeneration	optic nerve atrophy
Availability	Mouse Genotype	gliosis	decreased amacrine cell number	retina ganglion cell degeneration	abnormal optic disk morphology	optic nerve cupping	optic nerve degeneration	optic nerve atrophy
	Tfap2b^{tm1b(EUCOMM)Wtsi}/Tfap2b⁺
	Tfap2b^tm1Rbu/Tfap2b^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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