TM4SF18 transmembrane 4 L six family member 18

Information
Symbol
TM4SF18
Type
protein-coding
Description
transmembrane 4 L six family member 18
Entrez Gene ID
116441
Genome
hg19
Position
chr3:149,036,285-149,051,423
Genome
hg38
Position
chr3:149,318,498-149,333,636
HGNC
HGNC:25181 HGNC
Ensembl
ENSG00000163762 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 24
Ranking
ClinVar
0
0
0
24
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
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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 L6D
HGNC HGNC:25181 HGNC
Ensembl ENSG00000163762 Ensembl
AllianceGenome HGNC:25181
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000470080.5 hg38 chr3 149,321,277 149,333,482 12,206
ENST00000296059.7 hg38 chr3 149,318,498 149,333,636 15,139
ENST00000296059.7 hg19 chr3 149,036,285 149,051,423 15,139
ENST00000470080.5 hg19 chr3 149,039,064 149,051,269 12,206
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