TRIM26 tripartite motif containing 26

Information
Symbol
TRIM26
Type
protein-coding
Description
tripartite motif containing 26
Entrez Gene ID
7726
Genome
hg19
Position
chr6:30,152,232-30,181,183
Genome
hg38
Position
chr6:30,184,455-30,213,406
MIM
600830 OMIM
HGNC
HGNC:12962 HGNC
Ensembl
ENSG00000234127 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
not provided 9 0
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
48
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
SYNONYM AFP
SYNONYM RNF95
SYNONYM ZNF173
MIM 600830 OMIM
HGNC HGNC:12962 HGNC
Ensembl ENSG00000234127 Ensembl
AllianceGenome HGNC:12962
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000453195.5 hg38 chr6 30,184,455 30,213,427 28,973
ENST00000437089.5 hg38 chr6 30,184,455 30,204,765 20,311
ENST00000454678.7 hg38 chr6 30,184,455 30,213,406 28,952
ENST00000437089.5 hg19 chr6 30,152,232 30,172,542 20,311
ENST00000454678.7 hg19 chr6 30,152,232 30,181,183 28,952
ENST00000453195.5 hg19 chr6 30,152,232 30,181,204 28,973
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