TM7SF2 transmembrane 7 superfamily member 2

Information
Symbol
TM7SF2
Type
protein-coding
Description
transmembrane 7 superfamily member 2
Entrez Gene ID
7108
Genome
hg19
Position
chr11:64,879,344-64,883,702
Genome
hg38
Position
chr11:65,111,872-65,116,230
MIM
603414 OMIM
HGNC
HGNC:11863 HGNC
Ensembl
ENSG00000149809 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
52
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 :
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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 ANG1
SYNONYM C14SR
SYNONYM DHCR14A
SYNONYM NET47
MIM 603414 OMIM
HGNC HGNC:11863 HGNC
Ensembl ENSG00000149809 Ensembl
AllianceGenome HGNC:11863
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000279263.14 hg38 chr11 65,111,872 65,116,230 4,359
ENST00000345348.9 hg38 chr11 65,111,884 65,116,235 4,352
ENST00000279263.14 hg19 chr11 64,879,344 64,883,702 4,359
ENST00000345348.9 hg19 chr11 64,879,356 64,883,707 4,352
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