ARX

GENE INFORMATION

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Gene name

ARX (HGNC Symbol)

Synonyms

CT121, EIEE1, ISSX, MRX29, MRX32, MRX33, MRX36, MRX38, MRX43, MRX54, MRX76, MRX87, MRXS1, PRTS

Description

aristaless related homeobox (HGNC Symbol)

Entrez gene summary

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]

Chromosome

X (Chromosome progress)

Cytoband

p21.3

Chromosome location (bp)

25021811 - 25034065

Ensembl

ENSG00000004848 (version 73.37)

Entrez gene

170302

UniProt

Q96QS3 (UniProt - Evidence at protein level)

neXtProt

NX_Q96QS3

Antibodypedia

ARX antibodies
 

PROTEIN VIEW

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ARX-001
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

ARX-001 ENSP00000368332
ENST00000379044
Q96QS3
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