TRIM5 tripartite motif containing 5

Information
Symbol
TRIM5
Type
protein-coding
Description
tripartite motif containing 5
Entrez Gene ID
85363
Genome
hg19
Position
chr11:5,684,425-5,706,304
Genome
hg38
Position
chr11:5,663,195-5,685,074
MIM
608487 OMIM
HGNC
HGNC:16276 HGNC
Ensembl
ENSG00000132256 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 40
Likely benign 0 46
Uncertain significance 0 288
Ranking
ClinVar
0
0
2
370
2
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 RNF88
SYNONYM TRIM5alpha
MIM 608487 OMIM
HGNC HGNC:16276 HGNC
Ensembl ENSG00000132256 Ensembl
AllianceGenome HGNC:16276
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000682968.1 hg38 chr11 5,663,666 5,685,099 21,434
ENST00000380027.5 hg38 chr11 5,663,563 5,872,358 208,796
ENST00000396847.7 hg38 chr11 5,663,617 5,685,042 21,426
ENST00000684655.1 hg38 chr11 5,663,572 5,685,097 21,526
ENST00000380034.8 hg38 chr11 5,663,195 5,685,074 21,880
ENST00000380034.8 hg19 chr11 5,684,425 5,706,304 21,880
ENST00000380027.5 hg19 chr11 5,684,793 5,893,588 208,796
ENST00000684655.1 hg19 chr11 5,684,802 5,706,327 21,526
ENST00000396847.7 hg19 chr11 5,684,847 5,706,272 21,426
ENST00000682968.1 hg19 chr11 5,684,896 5,706,329 21,434
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