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Symbol Name ID |
Kcnj2
potassium inwardly-rectifying channel, subfamily J, member 2 MGI:104744 |
| Darker colors indicate more annotations |
| Human Phenotypes | Scaphocephaly |
Short mandibular rami |
Micrognathia |
Antegonial notching of mandible |
Hypoplasia of the maxilla |
Prominent frontal sinuses |
Malar flattening |
Microcephaly |
Abnormal facial shape |
Facial asymmetry |
Triangular face |
Preauricular pit |
Broad forehead |
Thin upper lip vermilion |
Cleft palate |
High palate |
Abnormality of the dentition |
Oligodontia |
Delayed eruption of permanent teeth |
Persistence of primary teeth |
Enamel hypoplasia |
Abnormality of dental color |
Dental crowding |
Bulbous nose |
Wide nasal bridge |
Blepharophimosis |
Short palpebral fissure |
| Disease(s) Associated with KCNJ2 | |||||||||||||||||||||||||||
| Andersen-Tawil syndrome |
| Mouse Phenotypes | decreased maxillary shelf size |
narrow maxilla |
small vomer bone |
palatal shelves fail to meet at midline |
cleft secondary palate |
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| Availability | Mouse Genotype | |||||
| Kcnj2tm1Swz/Kcnj2tm1Swz | ||||||
| Kcnj2tm1Swz/Kcnj2+ | ||||||
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 09/03/2024 MGI 6.24 |
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