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Symbol
Name
ID
Stk11
serine/threonine kinase 11
MGI:1341870
Phenotype annotations related to craniofacial
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
absent first pharyngeal arch
first pharyngeal arch hypoplasia
Availability Mouse Genotype
Stk11tm1Tpm/Stk11tm1Tpm
Stk11tm2.1Tpm/Stk11tm2.1Tpm

Contributing Projects:
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
02/18/2020
MGI 6.14
The Jackson Laboratory