|
Symbol Name ID |
Ptch1
patched 1 MGI:105373 |
| Darker colors indicate more annotations |
| Human Phenotypes | Shallow orbits |
Cataract |
Iris coloboma |
Chorioretinal coloboma |
Optic atrophy |
Retinopathy |
Cyclopia |
Deeply set eye |
Hypertelorism |
Hypotelorism |
Anophthalmia |
Microphthalmia |
Bilateral microphthalmos |
Strabismus |
Glaucoma |
Ptosis |
| Disease(s) Associated with PTCH1 | ||||||||||||||||
| holoprosencephaly | ||||||||||||||||
| holoprosencephaly 7 | ||||||||||||||||
| nevoid basal cell carcinoma syndrome | ||||||||||||||||
| nevoid basal cell carcinoma syndrome 1 |
| Mouse Phenotypes | absent optic vesicle |
ocular hypertelorism |
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| Availability | Mouse Genotype | ||
| Ptch1mes/Ptch1mes | |||
| 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 04/30/2024 MGI 6.23 |
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