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Symbol
Name
ID
Tfap2a
transcription factor AP-2, alpha
MGI:104671
Phenotype annotations related to growth/size/body
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
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)
Tfap2atm1Hsv/Tfap2atm2Will
H2az2Tg(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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory