TSPAN16 tetraspanin 16

Information
Symbol
TSPAN16
Type
protein-coding
Description
tetraspanin 16
Entrez Gene ID
26526
Genome
hg19
Position
chr19:11,406,824-11,437,672
Genome
hg38
Position
chr19:11,296,148-11,326,996
MIM
617580 OMIM
HGNC
HGNC:30725 HGNC
Ensembl
ENSG00000130167 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 24
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 TM-8
SYNONYM TM4-B
SYNONYM TM4SF16
MIM 617580 OMIM
HGNC HGNC:30725 HGNC
Ensembl ENSG00000130167 Ensembl
AllianceGenome HGNC:30725
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000621731.4 hg38 chr19 11,296,139 11,306,603 10,465
ENST00000592955.5 hg38 chr19 11,296,160 11,315,967 19,808
ENST00000590327.6 hg38 chr19 11,296,160 11,315,967 19,808
ENST00000316737.5 hg38 chr19 11,296,148 11,326,996 30,849
ENST00000621731.4 hg19 chr19 11,406,815 11,417,279 10,465
ENST00000316737.5 hg19 chr19 11,406,824 11,437,672 30,849
ENST00000590327.6 hg19 chr19 11,406,836 11,426,643 19,808
ENST00000592955.5 hg19 chr19 11,406,836 11,426,643 19,808
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