RHOXF2 Rhox homeobox family member 2

Information
Symbol
RHOXF2
Type
protein-coding
Description
Rhox homeobox family member 2
Entrez Gene ID
84528
Genome
hg19
Position
chrX:119,292,519-119,299,536
Genome
hg38
Position
chrX:120,158,613-120,165,630
MIM
300447 OMIM
HGNC
HGNC:30011 HGNC
Ensembl
ENSG00000131721 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 10
Conflicting classifications of pathogenicity 0 2
not provided 6 0
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
30
2
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 CT107
SYNONYM PEPP-2
SYNONYM PEPP2
SYNONYM THG1
MIM 300447 OMIM
HGNC HGNC:30011 HGNC
Ensembl ENSG00000131721 Ensembl
AllianceGenome HGNC:30011
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000371388.5 hg38 chrX 120,158,613 120,165,630 7,018
ENST00000371388.5 hg19 chrX 119,292,519 119,299,536 7,018
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