ARX
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human X chromosome[12]
- Cytogenetic location
- Xp21.3[20]
- Expressed in
- left ovary, right ovary, ventricular zone, vastus lateralis muscle, germinal epithelium, endothelial cell, bronchial epithelial cell, Brodmann area 23, biceps brachii, cingulate gyrus[21][22][23][24][25][26][27][28][29][30]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- corpus callosum agenesis-abnormal genitalia syndrome, X-linked lissencephaly with abnormal genitalia, intellectual disability, X-linked, with or without seizures, Arx-related, infantile epileptic-dyskinetic encephalopathy, X-linked spasticity-intellectual disability-epilepsy syndrome, non-syndromic X-linked intellectual disability[13][14][15][16][17][18]
- HomoloGene ID
- 68998[3]
- Strand orientation
- reverse strand[19]
🏷️ Also known as
en aristaless related homeobox
en ARX
en CT121
en EIEE1
en ISSX
en MRX29
en MRX32
en MRX33
en MRX36
en MRX38
en MRX43
en MRX54
en MRX76
en MRX87
en MRXS1
en PRTS
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000004848
- Ensembl transcript ID
- ENST00000379044, ENST00000636609, ENST00000636885, ENST00000637394, ENST00000637993
- Entrez Gene ID
- 170302
- Exact match
- identifiers.org
- Freebase ID
- /m/02z4pty
- HGNC ID
- 18060
- HGNC gene symbol
- ARX
- OMIM ID
- 300382
- RefSeq RNA ID
- NM_139058
- UMLS CUI
- C1425272
Press Enter · cited answer in seconds