TNFRSF11A TNF receptor superfamily member 11a

Information
Symbol
TNFRSF11A
Type
protein-coding
Description
TNF receptor superfamily member 11a
Entrez Gene ID
8792
Genome
hg19
Position
chr18:59,992,543-60,058,521
Genome
hg38
Position
chr18:62,325,310-62,391,288
MIM
603499 OMIM
HGNC
HGNC:11908 HGNC
Ensembl
ENSG00000141655 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 38
Likely pathogenic 1 16
Benign 2 108
Likely benign 0 350
Conflicting classifications of pathogenicity 0 56
Uncertain significance 0 686
Ranking
ClinVar
0
0
134
1,028
8
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 CD265
SYNONYM FEO
SYNONYM LOH18CR1
SYNONYM ODFR
SYNONYM OFE
SYNONYM OPTB7
SYNONYM OSTS
SYNONYM PDB2
SYNONYM RANK
SYNONYM TRANCE-R
SYNONYM TRANCER
MIM 603499 OMIM
HGNC HGNC:11908 HGNC
Ensembl ENSG00000141655 Ensembl
AllianceGenome HGNC:11908
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000269485.11 hg38 chr18 62,325,287 62,387,659 62,373
ENST00000586569.3 hg38 chr18 62,325,310 62,391,288 65,979
ENST00000269485.11 hg19 chr18 59,992,520 60,054,892 62,373
ENST00000586569.3 hg19 chr18 59,992,543 60,058,521 65,979
Genome browser