TRIM11 tripartite motif containing 11

Information
Symbol
TRIM11
Type
protein-coding
Description
tripartite motif containing 11
Entrez Gene ID
81559
Genome
hg19
Position
chr1:228,581,377-228,594,536
Genome
hg38
Position
chr1:228,393,676-228,406,835
MIM
607868 OMIM
HGNC
HGNC:16281 HGNC
Ensembl
ENSG00000154370 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
40
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 BIA1
SYNONYM RNF92
MIM 607868 OMIM
HGNC HGNC:16281 HGNC
Ensembl ENSG00000154370 Ensembl
AllianceGenome HGNC:16281
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000493030.6 hg38 chr1 228,393,673 228,405,904 12,232
ENST00000284551.11 hg38 chr1 228,393,676 228,406,835 13,160
ENST00000366699.3 hg38 chr1 228,395,534 228,406,800 11,267
ENST00000493030.6 hg19 chr1 228,581,374 228,593,605 12,232
ENST00000284551.11 hg19 chr1 228,581,377 228,594,536 13,160
ENST00000366699.3 hg19 chr1 228,583,235 228,594,501 11,267
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