TMEM169 transmembrane protein 169

Information
Symbol
TMEM169
Type
protein-coding
Description
transmembrane protein 169
Entrez Gene ID
92691
Genome
hg19
Position
chr2:216,946,618-216,967,506
Genome
hg38
Position
chr2:216,081,895-216,102,783
HGNC
HGNC:25130 HGNC
Ensembl
ENSG00000163449 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 56
Ranking
ClinVar
0
0
0
56
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
HGNC HGNC:25130 HGNC
Ensembl ENSG00000163449 Ensembl
AllianceGenome HGNC:25130
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000295658.8 hg38 chr2 216,081,895 216,102,783 20,889
ENST00000437356.7 hg38 chr2 216,081,919 216,102,783 20,865
ENST00000454545.5 hg38 chr2 216,081,866 216,102,782 20,917
ENST00000406027.2 hg38 chr2 216,081,919 216,102,382 20,464
ENST00000454545.5 hg19 chr2 216,946,589 216,967,505 20,917
ENST00000295658.8 hg19 chr2 216,946,618 216,967,506 20,889
ENST00000406027.2 hg19 chr2 216,946,642 216,967,105 20,464
ENST00000437356.7 hg19 chr2 216,946,642 216,967,506 20,865
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