Symbol Name ID |
Trp53
transformation related protein 53 MGI:98834 |
Darker colors indicate more annotations |
Human Phenotypes | Central retinal vessel vascular tortuosity |
Neoplasia of the nasopharynx |
Disease(s) Associated with TP53 | ||
Leber hereditary optic neuropathy | ||
nasopharynx carcinoma |
Mouse Phenotypes | abnormal craniofacial morphology |
short mandible |
square face |
cleft upper lip |
oral leukoplakia |
cleft palate |
abnormal tongue morphology |
protruding tongue |
abnormal outer ear morphology |
increased ear pigmentation |
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Availability | Mouse Genotype | ||||||||||
Trp53tm1.1Tldo/Trp53tm1.1Tldo | |||||||||||
Trp53tm1Att/Trp53+ Tg(KRT5-cre)5132Jlj/0 (conditional) |
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Tg(CMV-cre)1Cgn/0 Trp53tm4Att/Trp53+ (conditional) |
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 |
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