TSPAN7 tetraspanin 7

Information
Symbol
TSPAN7
Type
protein-coding
Description
tetraspanin 7
Entrez Gene ID
7102
Genome
hg19
Position
chrX:38,420,795-38,548,172
Genome
hg38
Position
chrX:38,561,542-38,688,918
MIM
300096 OMIM
HGNC
HGNC:11854 HGNC
Ensembl
ENSG00000156298 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Benign 0 6
Likely benign 0 10
Conflicting classifications of pathogenicity 0 4
not provided 6 0
Uncertain significance 0 34
Ranking
ClinVar
0
0
4
42
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
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 A15
SYNONYM CCG-B7
SYNONYM CD231
SYNONYM DXS1692E
SYNONYM MRX58
SYNONYM MXS1
SYNONYM TALLA-1
SYNONYM TM4SF2
SYNONYM TM4SF2b
SYNONYM XLID58
MIM 300096 OMIM
HGNC HGNC:11854 HGNC
Ensembl ENSG00000156298 Ensembl
AllianceGenome HGNC:11854
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000378482.7 hg38 chrX 38,561,542 38,688,918 127,377
ENST00000286824.6 hg38 chrX 38,561,544 38,688,397 126,854
ENST00000378482.7 hg19 chrX 38,420,795 38,548,172 127,378
ENST00000286824.6 hg19 chrX 38,420,797 38,547,651 126,855
Genome browser