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Symbol Name ID |
Tfap2b
transcription factor AP-2 beta MGI:104672 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypertelorism |
Strabismus |
Ptosis |
| Disease(s) Associated with TFAP2B | |||
| Char syndrome |
| Mouse Phenotypes | cornea vascularization |
decreased amacrine cell number |
retina ganglion cell degeneration |
abnormal optic disk morphology |
optic nerve cupping |
optic nerve degeneration |
optic nerve atrophy |
abnormal eye morphology |
abnormal iridocorneal angle |
abnormal ciliary body morphology |
iris synechia |
anterior iris synechia |
abnormal cornea morphology |
absent cornea endothelium |
abnormal cornea epithelium morphology |
decreased cornea epithelium thickness |
abnormal cornea stroma morphology |
cornea deposits |
fused cornea and lens |
abnormal eye anterior chamber morphology |
abnormal lens epithelium morphology |
anterior subcapsular cataract |
thin retina inner plexiform layer |
decreased total retina thickness |
eye opacity |
ocular hypertension |
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| Availability | Mouse Genotype | ||||||||||||||||||||||||||
| Tfap2btm1b(EUCOMM)Wtsi/Tfap2b+ | |||||||||||||||||||||||||||
| Tfap2btm1Rbu/Tfap2btm2Will H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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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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last database update 04/30/2024 MGI 6.23 |
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