Name

ARX Gene

aristaless related homeobox

This gene is a homeobox-containing gene expressed during development. The expressed protein contains two conserved domains, a C-peptide (or aristaless domain) and the prd-like class homeobox domain. It is a member of the group-II aristaless-related protein family whose members are expressed primarily in the central and/or peripheral nervous system. This gene is thought to be involved in CNS development. Mutations in this gene cause X-linked mental retardation and epilepsy. [provided by RefSeq, Jul 2008]

arx Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term arx in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

X-linked mental retardation, with or without seizures, ARX-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset.

ARX_KO_GSE12609_3_mouse_brain (subpallium, Pou3f-expressing cells) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the ARX_KO_GSE12609_3_mouse_brain (subpallium, Pou3f-expressing cells) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.