TMEM145 transmembrane protein 145

Information
Symbol
TMEM145
Type
protein-coding
Description
transmembrane protein 145
Entrez Gene ID
284339
Genome
hg19
Position
chr19:42,817,529-42,829,205
Genome
hg38
Position
chr19:42,313,377-42,325,053
HGNC
HGNC:26912 HGNC
Ensembl
ENSG00000167619 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 1 0
Uncertain significance 0 62
Ranking
ClinVar
0
0
0
64
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
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:26912 HGNC
Ensembl ENSG00000167619 Ensembl
AllianceGenome HGNC:26912
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000301204.8 hg38 chr19 42,313,309 42,325,064 11,756
ENST00000673205.1 hg38 chr19 42,313,309 42,325,064 11,756
ENST00000598766.1 hg38 chr19 42,313,377 42,321,789 8,413
ENST00000673187.1 hg38 chr19 42,313,377 42,325,053 11,677
ENST00000301204.8 hg19 chr19 42,817,461 42,829,216 11,756
ENST00000673205.1 hg19 chr19 42,817,461 42,829,216 11,756
ENST00000598766.1 hg19 chr19 42,817,529 42,825,941 8,413
ENST00000673187.1 hg19 chr19 42,817,529 42,829,205 11,677
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