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Symbol Name ID |
Scube3
signal peptide, CUB domain, EGF-like 3 MGI:3045253 |
| Darker colors indicate more annotations |
| Human Phenotypes | Bicoronal synostosis |
Microcephaly |
Long face |
Triangular face |
Pointed chin |
Short chin |
High forehead |
Thick vermilion border |
Cleft palate |
Hypodontia |
Oligodontia |
Enamel hypoplasia |
Misalignment of incisors |
Dental crowding |
Pierre-Robin sequence |
Prominent nasal bridge |
Long nose |
| Disease(s) Associated with SCUBE3 | |||||||||||||||||
| short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies |
| Mouse Phenotypes | abnormal temporal bone morphology |
abnormal middle ear ossicle morphology |
small incus |
abnormal malleus morphology |
abnormal malleus head morphology |
small middle ear ossicles |
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| Availability | Mouse Genotype | ||||||
| Scube3m1Mhda/Scube3m1Mhda | |||||||
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 04/09/2024 MGI 6.23 |
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