TSPAN32 tetraspanin 32

Information
Symbol
TSPAN32
Type
protein-coding
Description
tetraspanin 32
Entrez Gene ID
10077
Genome
hg19
Position
chr11:2,323,243-2,339,434
Genome
hg38
Position
chr11:2,302,013-2,318,204
MIM
603853 OMIM
HGNC
HGNC:13410 HGNC
Ensembl
ENSG00000064201 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 4
Uncertain significance 0 62
Ranking
ClinVar
0
0
0
68
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 :
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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 ART1
SYNONYM PHEMX
SYNONYM PHMX
SYNONYM TSSC6
MIM 603853 OMIM
HGNC HGNC:13410 HGNC
Ensembl ENSG00000064201 Ensembl
AllianceGenome HGNC:13410
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000451520.6 hg38 chr11 2,302,723 2,318,142 15,420
ENST00000381121.7 hg38 chr11 2,302,150 2,318,142 15,993
ENST00000182290.9 hg38 chr11 2,302,013 2,318,204 16,192
ENST00000612299.4 hg38 chr11 2,302,013 2,318,200 16,188
ENST00000182290.9 hg19 chr11 2,323,243 2,339,434 16,192
ENST00000381121.7 hg19 chr11 2,323,380 2,339,372 15,993
ENST00000451520.6 hg19 chr11 2,323,953 2,339,372 15,420
ENST00000612299.4 hg19 chr11 2,323,243 2,339,430 16,188
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