TSPAN11 tetraspanin 11

Information
Symbol
TSPAN11
Type
protein-coding
Description
tetraspanin 11
Entrez Gene ID
441631
Genome
hg19
Position
chr12:31,079,892-31,149,537
Genome
hg38
Position
chr12:30,926,958-30,996,602
HGNC
HGNC:30795 HGNC
Ensembl
ENSG00000110900 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
26
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 VSSW1971
HGNC HGNC:30795 HGNC
Ensembl ENSG00000110900 Ensembl
AllianceGenome HGNC:30795
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000261177.10 hg38 chr12 30,926,958 30,996,602 69,645
ENST00000545802.1 hg38 chr12 30,926,428 30,955,260 28,833
ENST00000535215.5 hg38 chr12 30,926,904 30,992,123 65,220
ENST00000546076.6 hg38 chr12 30,926,748 30,996,599 69,852
ENST00000545802.1 hg19 chr12 31,079,362 31,108,194 28,833
ENST00000546076.6 hg19 chr12 31,079,682 31,149,534 69,853
ENST00000535215.5 hg19 chr12 31,079,838 31,145,058 65,221
ENST00000261177.10 hg19 chr12 31,079,892 31,149,537 69,646
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