HSPB2-C11orf52 HSPB2-C11orf52 readthrough (NMD candidate)

Information
Symbol
HSPB2-C11orf52
Type
ncRNA
Description
HSPB2-C11orf52 readthrough (NMD candidate)
Entrez Gene ID
100528019
Genome
hg19
Position
chr11:111,783,460-111,789,574
Genome
hg38
Position
chr11:111,912,736-111,918,850
HGNC
HGNC:41996 HGNC
Ensembl
ENSG00000254445 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 16
Ranking
ClinVar
0
0
0
18
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
[No Data.]
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 C11orf52
HGNC HGNC:41996 HGNC
Ensembl ENSG00000254445 Ensembl
AllianceGenome HGNC:41996
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000527616.1 hg38 chr11 111,912,736 111,918,850 6,115
ENST00000527616.1 hg19 chr11 111,783,460 111,789,574 6,115
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