TRIM4 tripartite motif containing 4

Information
Symbol
TRIM4
Type
protein-coding
Description
tripartite motif containing 4
Entrez Gene ID
89122
Genome
hg19
Position
chr7:99,488,036-99,517,154
Genome
hg38
Position
chr7:99,890,413-99,919,531
HGNC
HGNC:16275 HGNC
Ensembl
ENSG00000146833 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 2 2
Uncertain significance 0 66
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
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 RNF87
HGNC HGNC:16275 HGNC
Ensembl ENSG00000146833 Ensembl
AllianceGenome HGNC:16275
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000354241.5 hg38 chr7 99,901,166 99,919,493 18,328
ENST00000349062.7 hg38 chr7 99,890,403 99,919,530 29,128
ENST00000355947.6 hg38 chr7 99,890,413 99,919,531 29,119
ENST00000349062.7 hg19 chr7 99,488,026 99,517,153 29,128
ENST00000355947.6 hg19 chr7 99,488,036 99,517,154 29,119
ENST00000354241.5 hg19 chr7 99,498,789 99,517,116 18,328
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