TNFSF11 TNF superfamily member 11

Information
Symbol
TNFSF11
Type
protein-coding
Description
TNF superfamily member 11
Entrez Gene ID
8600
Genome
hg19
Position
chr13:43,148,288-43,182,149
Genome
hg38
Position
chr13:42,574,152-42,608,013
MIM
602642 OMIM
HGNC
HGNC:11926 HGNC
Ensembl
ENSG00000120659 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 2
Benign 0 42
Likely benign 0 158
Conflicting classifications of pathogenicity 0 14
Uncertain significance 0 216
Ranking
ClinVar
0
0
54
358
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 :
Search word :
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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 CD254
SYNONYM ODF
SYNONYM OPGL
SYNONYM OPTB2
SYNONYM RANKL
SYNONYM TNLG6B
SYNONYM TRANCE
SYNONYM hRANKL2
SYNONYM sOdf
MIM 602642 OMIM
HGNC HGNC:11926 HGNC
Ensembl ENSG00000120659 Ensembl
AllianceGenome HGNC:11926
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000398795.7 hg38 chr13 42,574,152 42,608,013 33,862
ENST00000358545.6 hg38 chr13 42,562,736 42,607,174 44,439
ENST00000358545.6 hg19 chr13 43,136,872 43,181,310 44,439
ENST00000398795.7 hg19 chr13 43,148,288 43,182,149 33,862
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