Symbol Name ID |
Tfap2a
transcription factor AP-2, alpha MGI:104671 |
Darker colors indicate more annotations |
Human Phenotypes | Low posterior hairline |
Branchial anomaly |
Short neck |
Duplication of internal organs |
Intrauterine growth retardation |
Postnatal growth retardation |
Disease(s) Associated with TFAP2A | ||||||
branchiooculofacial syndrome |
Mouse Phenotypes | malocclusion |
abnormal nasal bone morphology |
absent nasal bone |
broad nasal bone |
short nasal bone |
abnormal palatal shelf fusion at midline |
abnormal facial morphology |
abnormal facial skin morphology |
abnormal periorbital skin morphology |
abnormal secondary palate morphology |
cleft palate |
absent mouth |
abnormal nasal septum cartilage morphology |
absent snout |
narrow snout |
short snout |
facial cleft |
midline facial cleft |
absent outer ear |
decreased body weight |
thoracoabdominoschisis |
abnormal ventral body wall morphology |
abnormal head morphology |
decreased body size |
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Availability | Mouse Genotype | ||||||||||||||||||||||||
Tfap2aMhdador/Tfap2aMhdador | |||||||||||||||||||||||||
Tfap2atm1.1Hsv/Tfap2atm1.1Hsv | |||||||||||||||||||||||||
Tfap2atm1Hsv/Tfap2atm1Hsv | |||||||||||||||||||||||||
Tfap2atm1Jae/Tfap2atm1Jae | |||||||||||||||||||||||||
Tfap2atm1Will/Tfap2atm1Will | |||||||||||||||||||||||||
Tfap2atm1Jae/Tfap2a+ | |||||||||||||||||||||||||
Tfap2atm1Will/Tfap2atm2.1Will | |||||||||||||||||||||||||
Tfap2atm2Will/Tfap2atm2Will HhatTg(TFAP2A-cre)1Will/0 (conditional) |
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Tfap2atm1Hsv/Tfap2atm2Will H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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 04/16/2024 MGI 6.23 |
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