FOXR2 forkhead box R2

Information
Symbol
FOXR2
Type
protein-coding
Description
forkhead box R2
Entrez Gene ID
139628
Genome
hg19
Position
chrX:55,649,833-55,652,625
Genome
hg38
Position
chrX:55,623,400-55,626,192
MIM
300949 OMIM
HGNC
HGNC:30469 HGNC
Ensembl
ENSG00000189299 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
not provided 6 0
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
40
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
SYNONYM FOXN6
MIM 300949 OMIM
HGNC HGNC:30469 HGNC
Ensembl ENSG00000189299 Ensembl
AllianceGenome HGNC:30469
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000339140.5 hg38 chrX 55,623,400 55,626,192 2,793
ENST00000339140.5 hg19 chrX 55,649,833 55,652,625 2,793
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