Symbol Name ID |
Ptch1
patched 1 MGI:105373 |
Darker colors indicate more annotations |
Human Phenotypes | Ventricular septal defect |
Tetralogy of Fallot |
Abnormal pulmonary valve morphology |
Cardiac fibroma |
Cardiac rhabdomyoma |
Abnormal aortic morphology |
Arrhythmia |
Abnormality of the spleen |
Disease(s) Associated with PTCH1 | ||||||||
holoprosencephaly | ||||||||
nevoid basal cell carcinoma syndrome | ||||||||
nevoid basal cell carcinoma syndrome 1 |
Mouse Phenotypes | abnormal vascular development |
abnormal heart development |
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Availability | Mouse Genotype | ||
Ptch1tm1Mps/Ptch1tm1Mps | |||
Ptch1wig/Ptch1wig |
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 |
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