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Symbol Name ID |
Gli2
GLI-Kruppel family member GLI2 MGI:95728 |
| Darker colors indicate more annotations |
| Human Phenotypes | Short neck |
Short stature |
| Disease(s) Associated with GLI2 | ||
| Culler-Jones syndrome | ||
| holoprosencephaly 9 |
| Mouse Phenotypes | absent lower incisors |
absent upper incisors |
absent maxillary shelf |
absent palatine bone horizontal plate |
abnormal palatal shelf elevation |
abnormal palatal shelf fusion at midline |
cleft secondary palate |
abnormal head shape |
decreased embryo size |
microcephaly |
decreased body size |
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| Availability | Mouse Genotype | |||||||||||
| Gli2tm1Alj/Gli2tm1Alj | ||||||||||||
| Gli2tm2.1(Gli3)Blnw/Gli2tm2.1(Gli3)Blnw | ||||||||||||
| En1tm2(cre)Gld/En1+ Gli2tm1Alj/Gli2tm6Alj (conditional) |
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| Gt(ROSA)26Sortm2(Gli2*)Flng/Gt(ROSA)26Sor+ Tg(Col2a1-cre)3Amc/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 04/16/2024 MGI 6.23 |
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