|
Symbol Name ID |
Ostm1
osteopetrosis associated transmembrane protein 1 MGI:2655574 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cranial hyperostosis |
Micrognathia |
Microcephaly |
Square face |
Facial palsy |
Long philtrum |
Gingival overgrowth |
| Disease(s) Associated with OSTM1 | |||||||
| autosomal recessive osteopetrosis 5 |
| Mouse Phenotypes | abnormal mental foramen morphology |
abnormal incisor morphology |
short lower incisors |
absent incisors |
short incisors |
abnormal molar morphology |
abnormal molar crown morphology |
abnormal molar root morphology |
abnormal dentin mineralization |
failure of tooth eruption |
abnormal maxilla morphology |
abnormal maxillary zygomatic process morphology |
short snout |
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| Availability | Mouse Genotype | |||||||||||||
| Ostm1gl/Ostm1gl | ||||||||||||||
| Ostm1om/Ostm1om | ||||||||||||||
| Ostm1gl/Ostm1om | ||||||||||||||
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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