Symbol Name ID |
Arx
aristaless related homeobox MGI:1097716 |
Darker colors indicate more annotations |
Human Phenotypes | Hypomimic face |
Flexion contracture |
Camptodactyly |
Limb joint contracture |
Hypertonia |
Rigidity |
Extrapyramidal muscular rigidity |
Spasticity |
Lower limb spasticity |
Spastic tetraparesis |
Spastic tetraplegia |
Hypotonia |
Axial hypotonia |
Generalized hypotonia |
Neonatal hypotonia |
Frequent falls |
Poor head control |
Disease(s) Associated with ARX | |||||||||||||||||
corpus callosum agenesis-abnormal genitalia syndrome | |||||||||||||||||
developmental and epileptic encephalopathy 1 | |||||||||||||||||
non-syndromic X-linked intellectual disability ARX-related | |||||||||||||||||
Partington syndrome | |||||||||||||||||
syndromic X-linked intellectual disability Hedera type | |||||||||||||||||
X-linked lissencephaly 2 |
Mouse Phenotypes | myoclonus |
muscle spasm |
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Availability | Mouse Genotype | ||
Arxtm1.1Jno/Arxtm1.1Jno | |||
Arxtm1.1Ics/Y | |||
Arxtm1.1Jno/Y | |||
Arxtm4Kki/Y | |||
Arxtm5Kki/Y |
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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