TRIM21 tripartite motif containing 21

Information
Symbol
TRIM21
Type
protein-coding
Description
tripartite motif containing 21
Entrez Gene ID
6737
Genome
hg19
Position
chr11:4,406,127-4,414,932
Genome
hg38
Position
chr11:4,384,897-4,393,702
MIM
109092 OMIM
HGNC
HGNC:11312 HGNC
Ensembl
ENSG00000132109 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 8
Uncertain significance 0 32
Ranking
ClinVar
0
0
0
44
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 RNF81
SYNONYM RO52
SYNONYM Ro/SSA
SYNONYM SSA
SYNONYM SSA1
MIM 109092 OMIM
HGNC HGNC:11312 HGNC
Ensembl ENSG00000132109 Ensembl
AllianceGenome HGNC:11312
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000254436.8 hg38 chr11 4,384,897 4,393,702 8,806
ENST00000254436.8 hg19 chr11 4,406,127 4,414,932 8,806
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