ARX aristaless related homeobox

Information
Symbol
ARX
Type
protein-coding
Description
aristaless related homeobox
Entrez Gene ID
170302
Genome
hg19
Position
chrX:25,021,811-25,034,082
Genome
hg38
Position
chrX:25,003,694-25,015,965
MIM
300382 OMIM
HGNC
HGNC:18060 HGNC
Ensembl
ENSG00000004848 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 36 188
Likely pathogenic 14 60
Benign 0 54
Likely benign 0 688
Conflicting classifications of pathogenicity 0 90
not provided 6 2
Uncertain significance 6 546
Ranking
ClinVar
0
0
206
1,256
34
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM CT121
SYNONYM EIEE1
SYNONYM ISSX
SYNONYM MRX29
SYNONYM MRX32
SYNONYM MRX33
SYNONYM MRX36
SYNONYM MRX38
SYNONYM MRX43
SYNONYM MRX54
SYNONYM MRX76
SYNONYM MRX87
SYNONYM MRXS1
SYNONYM PRTS
MIM 300382 OMIM
HGNC HGNC:18060 HGNC
Ensembl ENSG00000004848 Ensembl
AllianceGenome HGNC:18060
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000379044.5 hg38 chrX 25,003,694 25,015,965 12,272
ENST00000379044.5 hg19 chrX 25,021,811 25,034,082 12,272
Genome browser