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Symbol Name ID |
Stk11
serine/threonine kinase 11 MGI:1341870 |
| Darker colors indicate more annotations |
| Human Phenotypes | Labial melanotic macule |
Abnormal pigmentation of the oral mucosa |
Oral melanotic macule |
Abnormality of the nose |
Nasal polyposis |
Neoplasm of the nose |
| Disease(s) Associated with STK11 | ||||||
| Peutz-Jeghers syndrome |
| Mouse Phenotypes | abnormal craniofacial morphology |
abnormal basicranium morphology |
small basisphenoid bone |
small cranium |
abnormal neurocranium morphology |
large anterior fontanelle |
small frontal bone |
small parietal bone |
abnormal sphenoid bone morphology |
small presphenoid bone |
small temporal bone squamous part |
abnormal alveolar process morphology |
short mandible |
small premaxilla |
small maxilla |
micrognathia |
abnormal nasal bone morphology |
abnormal palatine bone morphology |
small vomer bone |
absent first pharyngeal arch |
first pharyngeal arch hypoplasia |
cleft secondary palate |
short snout |
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| Availability | Mouse Genotype | |||||||||||||||||||||||
| Stk11tm1Tpm/Stk11tm1Tpm | ||||||||||||||||||||||||
| Stk11tm1.1Rdp/Stk11tm1.1Rdp Tg(PLAT-cre)116Sdu/0 (conditional) |
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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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