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Symbol Name ID |
Arx
aristaless related homeobox MGI:1097716 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Death in infancy |
| Disease(s) Associated with ARX | |
| X-linked lissencephaly 2 |
| Mouse Phenotypes | mortality/aging |
increased susceptibility to induced morbidity/mortality |
decreased survivor rate |
premature death |
neonatal lethality, complete penetrance |
postnatal lethality, complete penetrance |
postnatal lethality, incomplete penetrance |
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| Availability | Mouse Genotype | |||||||
| Arxtm1Kki/Y | ||||||||
| Arxtm1Pgr/Y | ||||||||
| Arxtm2Kki/Y | ||||||||
| Arxtm3Kki/Y | * | |||||||
| Arxtm4Kki/Y | ||||||||
| Arxtm5Kki/Y | ||||||||
| Arxtm1Gldn/Y Tg(mI56i-cre,-EGFP)1Kc/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 05/19/2026 MGI 6.24 |
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