TRIM25 tripartite motif containing 25

Information
Symbol
TRIM25
Type
protein-coding
Description
tripartite motif containing 25
Entrez Gene ID
7706
Genome
hg19
Position
chr17:54,965,270-54,991,410
Genome
hg38
Position
chr17:56,887,909-56,914,049
MIM
600453 OMIM
HGNC
HGNC:12932 HGNC
Ensembl
ENSG00000121060 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 8
Uncertain significance 0 54
Ranking
ClinVar
0
0
0
68
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 EFP
SYNONYM RNF147
SYNONYM Z147
SYNONYM ZNF147
MIM 600453 OMIM
HGNC HGNC:12932 HGNC
Ensembl ENSG00000121060 Ensembl
AllianceGenome HGNC:12932
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000537230.3 hg38 chr17 56,890,668 56,914,032 23,365
ENST00000316881.9 hg38 chr17 56,887,909 56,914,049 26,141
ENST00000316881.9 hg19 chr17 54,965,270 54,991,410 26,141
ENST00000537230.3 hg19 chr17 54,968,029 54,991,393 23,365
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