Symbol Name ID |
Otx2
orthodenticle homeobox 2 MGI:97451 |
Darker colors indicate more annotations |
Human Phenotypes | Delayed puberty |
Short stature |
Pituitary dwarfism |
Growth delay |
Disease(s) Associated with OTX2 | ||||
panhypopituitarism | ||||
syndromic microphthalmia 5 |
Mouse Phenotypes | abnormal nasal capsule morphology |
absent nasal capsule |
abnormal facial morphology |
abnormal palate morphology |
absent tongue |
abnormal nasal cavity morphology |
abnormal nasal septum morphology |
abnormal vomeronasal organ morphology |
absent vomeronasal organ |
absent nasal septum |
abnormal olfactory epithelium morphology |
abnormal snout morphology |
short snout |
embryonic growth retardation |
decreased embryo size |
abnormal head morphology |
abnormal anterior head development |
microcephaly |
acephaly |
decreased body size |
postnatal growth retardation |
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Availability | Mouse Genotype | |||||||||||||||||||||
Otx2tm1Pas/Otx2tm1Pas | ||||||||||||||||||||||
Otx2tm1Sia/Otx2tm1Sia | ||||||||||||||||||||||
Otx2tm1Sla/Otx2tm1Sla | ||||||||||||||||||||||
Otx2tm2.1Imat/Otx2tm2.1Imat | ||||||||||||||||||||||
Otx2tm2Asim/Otx2tm2Asim | ||||||||||||||||||||||
Otx2tm3Tlam/Otx2tm3Tlam | ||||||||||||||||||||||
Otx2tm9Asim/Otx2tm9Asim | ||||||||||||||||||||||
Otx2tm10Asim/Otx2tm10Asim | ||||||||||||||||||||||
Otx2tm1Pas/Otx2tm2Asim | ||||||||||||||||||||||
Otx2tm1Sia/Otx2+ | ||||||||||||||||||||||
Otx2tm9Asim/Otx2tm11Asim | ||||||||||||||||||||||
Otx2tm10Asim/Otx2tm11Asim | ||||||||||||||||||||||
Otx2tm12.1Asim/Otx2tm11Asim | ||||||||||||||||||||||
Otx2tm1.1Tlam/Otx2tm2(cre/ERT2)Tlam (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 04/23/2024 MGI 6.23 |
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