TRIM59 tripartite motif containing 59

Information
Symbol
TRIM59
Type
protein-coding
Description
tripartite motif containing 59
Entrez Gene ID
286827
Genome
hg19
Position
chr3:160,153,291-160,167,574
Genome
hg38
Position
chr3:160,435,503-160,449,786
MIM
616148 OMIM
HGNC
HGNC:30834 HGNC
Ensembl
ENSG00000213186 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 70
Ranking
ClinVar
0
0
0
74
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 IFT80L
SYNONYM MRF1
SYNONYM RNF104
SYNONYM TRIM57
SYNONYM TSBF1
MIM 616148 OMIM
HGNC HGNC:30834 HGNC
Ensembl ENSG00000213186 Ensembl
AllianceGenome HGNC:30834
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000543469.1 hg38 chr3 160,432,445 160,448,937 16,493
ENST00000309784.9 hg38 chr3 160,435,503 160,449,786 14,284
ENST00000543469.1 hg19 chr3 160,150,233 160,166,725 16,493
ENST00000309784.9 hg19 chr3 160,153,291 160,167,574 14,284
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