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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Tfap2b
transcription factor AP-2 beta
MGI:104672
63 phenotypes from 4 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Tfap2bem1Fenli/Tfap2bem1Fenli
involves: C57BL/6
abnormal fetal ductus arteriosus morphology J:278067
abnormal kidney morphology J:278067
abnormal vascular smooth muscle physiology J:278067
normal craniofacial phenotype J:278067
dilated renal tubule J:278067
kidney cyst J:278067
kidney vascular congestion J:278067
normal limbs/digits/tail phenotype J:278067
neonatal lethality, complete penetrance J:278067
patent ductus arteriosus J:278067
Tfap2btm1b(EUCOMM)Wtsi/Tfap2b+
C57BL/6N-Tfap2btm1b(EUCOMM)Wtsi/Ieg
abnormal optic disk morphology J:211773
corneal deposits J:211773
increased grip strength J:211773
iris synechia J:211773
Tfap2btm1b(EUCOMM)Wtsi/Tfap2btm1b(EUCOMM)Wtsi
C57BL/6N-Tfap2btm1b(EUCOMM)Wtsi/Ieg
preweaning lethality, complete penetrance J:211773
Tfap2btm1Rbu/Tfap2b+
involves: 129S1/Sv * 129X1/SvJ
patent ductus arteriosus J:175832
postaxial polydactyly J:175832
Tfap2btm1Rbu/Tfap2btm1Rbu
129P2.129-Tfap2btm1Rbu
abnormal ion homeostasis J:83000
abnormal kidney physiology J:83000
decreased circulating calcium level J:83000
decreased urine calcium level J:83000
decreased urine osmolality J:83000
dilated proximal convoluted tubule J:83000
increased blood urea nitrogen level J:83000
increased circulating creatinine level J:83000
increased circulating parathyroid hormone level J:83000
increased circulating phosphate level J:83000
kidney cyst J:83000
muscle spasm J:83000
polydactyly J:83000
postnatal growth retardation J:83000
postnatal lethality, complete penetrance J:83000
scaly skin J:83000
tremors J:83000
Tfap2btm1Rbu/Tfap2btm1Rbu
involves: 129S1/Sv * 129X1/SvJ
abnormal pulmonary alveolar system morphology J:175832
congestive heart failure J:175832
neonatal lethality, incomplete penetrance J:175832
patent ductus arteriosus J:175832
postaxial polydactyly J:175832
pulmonary vascular congestion J:175832
Tfap2btm1Rbu/Tfap2btm1Rbu
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
increased kidney apoptosis J:42260
increased renal tubule apoptosis J:42260
kidney cyst J:42260
neonatal lethality, complete penetrance J:42260
small kidney J:42260
Tfap2btm1Rbu/Tfap2btm2Will
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J
abnormal ciliary body morphology J:234170
abnormal cornea morphology J:234170
abnormal corneal epithelium morphology J:234170
abnormal corneal stroma morphology J:234170
abnormal eye anterior chamber morphology J:234170
abnormal eye morphology J:234170
abnormal iridocorneal angle J:234170
abnormal lens epithelium morphology J:234170
abnormal optic disk morphology J:234170
absent corneal endothelium J:234170
anterior iris synechia J:234170
anterior subcapsular cataract J:234170
corneal vascularization J:234170
decreased amacrine cell number J:234170
decreased corneal epithelium thickness J:234170
decreased total retina thickness J:234170
eye opacity J:234170
fused cornea and lens J:234170
gliosis J:234170
ocular hypertension J:234170
optic nerve atrophy J:234170
optic nerve cupping J:234170
optic nerve degeneration J:234170
retina ganglion cell degeneration J:234170
thin retina inner plexiform layer J:234170

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
04/23/2024
MGI 6.23
The Jackson Laboratory