RXRA retinoid X receptor alpha

Information
Symbol
RXRA
Type
protein-coding
Description
retinoid X receptor alpha
Entrez Gene ID
6256
Genome
hg19
Position
chr9:137,218,301-137,332,431
Genome
hg38
Position
chr9:134,326,455-134,440,585
MIM
180245 OMIM
HGNC
HGNC:10477 HGNC
Ensembl
ENSG00000186350 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 6
Likely benign 0 4
Uncertain significance 0 26
Ranking
ClinVar
0
0
0
30
6
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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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 NR2B1
SYNONYM RXR-alpha
SYNONYM RXRalpha
MIM 180245 OMIM
HGNC HGNC:10477 HGNC
Ensembl ENSG00000186350 Ensembl
AllianceGenome HGNC:10477
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000672570.1 hg38 chr9 134,379,295 134,436,777 57,483
ENST00000481739.2 hg38 chr9 134,326,455 134,440,585 114,131
ENST00000481739.2 hg19 chr9 137,218,301 137,332,431 114,131
ENST00000672570.1 hg19 chr9 137,271,141 137,328,623 57,483
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