Symbol Name ID |
Ptch1
patched 1 MGI:105373 |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Cardiac rhabdomyoma |
Congenital diaphragmatic hernia |
Spasticity |
Hypotonia |
Muscle weakness |
Rhabdomyoma |
Disease(s) Associated with PTCH1 | ||||||
holoprosencephaly | ||||||
nevoid basal cell carcinoma syndrome 1 |
Mouse Phenotypes | abnormal tendon morphology |
increased rhabdomyosarcoma incidence |
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Availability | Mouse Genotype | ||
Ptch1mes/Ptch1mes | |||
Ptch1tm1.1Hahn/Ptch1+ | |||
Ptch1tm1Mps/Ptch1+ | |||
Ptch1tm1Zim/Ptch1+ | ! |
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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