TM9SF2 transmembrane 9 superfamily member 2

Information
Symbol
TM9SF2
Type
protein-coding
Description
transmembrane 9 superfamily member 2
Entrez Gene ID
9375
Genome
hg19
Position
chr13:100,151,210-100,215,588
Genome
hg38
Position
chr13:99,498,956-99,563,334
MIM
604678 OMIM
HGNC
HGNC:11865 HGNC
Ensembl
ENSG00000125304 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 44
Ranking
ClinVar
0
0
0
46
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 Lnc-PCIR
SYNONYM P76
MIM 604678 OMIM
HGNC HGNC:11865 HGNC
Ensembl ENSG00000125304 Ensembl
AllianceGenome HGNC:11865
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000642475.1 hg38 chr13 99,498,956 99,563,334 64,379
ENST00000376387.5 hg38 chr13 99,501,472 99,564,048 62,577
ENST00000642475.1 hg19 chr13 100,151,210 100,215,588 64,379
ENST00000376387.5 hg19 chr13 100,153,726 100,216,302 62,577
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