RAX2 retina and anterior neural fold homeobox 2

Information
Symbol
RAX2
Type
protein-coding
Description
retina and anterior neural fold homeobox 2
Entrez Gene ID
84839
Genome
hg19
Position
chr19:3,769,087-3,772,226
Genome
hg38
Position
chr19:3,769,089-3,772,228
MIM
610362 OMIM
HGNC
HGNC:18286 HGNC
Ensembl
ENSG00000173976 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 2
Benign 0 58
Likely benign 0 156
Conflicting classifications of pathogenicity 0 24
Uncertain significance 0 282
Ranking
ClinVar
0
0
56
426
4
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 :
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 ARMD6
SYNONYM CORD11
SYNONYM QRX
SYNONYM RAXL1
SYNONYM RP95
MIM 610362 OMIM
HGNC HGNC:18286 HGNC
Ensembl ENSG00000173976 Ensembl
AllianceGenome HGNC:18286
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000555978.5 hg38 chr19 3,769,089 3,772,211 3,123
ENST00000555633.3 hg38 chr19 3,769,089 3,772,228 3,140
ENST00000555978.5 hg19 chr19 3,769,087 3,772,209 3,123
ENST00000555633.3 hg19 chr19 3,769,087 3,772,226 3,140
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