Symbol Name ID |
Irf6
interferon regulatory factor 6 MGI:1859211 |
Darker colors indicate more annotations |
Human Phenotypes | Short neck |
Inguinal hernia |
Omphalocele |
Inferiorly positioned umbilicus |
Intrauterine growth retardation |
Disease(s) Associated with IRF6 | |||||
popliteal pterygium syndrome |
Mouse Phenotypes | abnormal tooth morphology |
taurodontia |
abnormal incisor morphology |
abnormal incisor color |
abnormal molar morphology |
abnormal molar crown morphology |
abnormal molar cusp morphology |
abnormal molar root morphology |
decreased molar number |
abnormal tooth development |
abnormal enamel development |
abnormal ameloblast morphology |
abnormal enamel mineralization |
abnormal enamel morphology |
abnormal enamel rod pattern |
reduced enamel thickness |
supernumerary teeth |
abnormal Hertwig epithelial root sheath morphology |
abnormal palatine bone horizontal plate morphology |
abnormal palate development |
failure of palatal shelf elevation |
palatal shelf fusion with tongue or mandible |
abnormal mouth morphology |
abnormal oral cavity morphology |
cleft secondary palate |
cleft palate |
glossopalatal ankylosis |
round snout |
short snout |
absent outer ear |
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Availability | Mouse Genotype | ||||||||||||||||||||||||||||||
Irf6clft1/Irf6clft1 | |||||||||||||||||||||||||||||||
Irf6Gt(OST398253)Lex/Irf6Gt(OST398253)Lex | |||||||||||||||||||||||||||||||
Irf6tm1Mjd/Irf6tm1Mjd | |||||||||||||||||||||||||||||||
Irf6tm1Mjd/Irf6+ | |||||||||||||||||||||||||||||||
Irf6tm1Bcsl/Irf6tm1Bcsl Pitx2tm4(cre)Jfm/Pitx2+ (conditional) |
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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