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) |
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 05/07/2024 MGI 6.23 |
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