RHOXF2B Rhox homeobox family member 2B

Information
Symbol
RHOXF2B
Type
protein-coding
Description
Rhox homeobox family member 2B
Entrez Gene ID
727940
Genome
hg19
Position
chrX:119,206,229-119,211,655
Genome
hg38
Position
chrX:120,072,264-120,077,690
HGNC
HGNC:33519 HGNC
Ensembl
ENSG00000203989 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 6 0
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
16
0
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
HGNC HGNC:33519 HGNC
Ensembl ENSG00000203989 Ensembl
AllianceGenome HGNC:33519
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000371402.5 hg38 chrX 120,072,264 120,077,690 5,427
ENST00000371402.5 hg19 chrX 119,206,229 119,211,655 5,427
Genome browser