TRIM22 tripartite motif containing 22

Information
Symbol
TRIM22
Type
protein-coding
Description
tripartite motif containing 22
Entrez Gene ID
10346
Genome
hg19
Position
chr11:5,711,020-5,732,093
Genome
hg38
Position
chr11:5,689,790-5,710,863
MIM
606559 OMIM
HGNC
HGNC:16379 HGNC
Ensembl
ENSG00000132274 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 20
Likely benign 0 14
Uncertain significance 0 40
Ranking
ClinVar
0
0
2
70
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 GPSTAF50
SYNONYM RNF94
SYNONYM STAF50
MIM 606559 OMIM
HGNC HGNC:16379 HGNC
Ensembl ENSG00000132274 Ensembl
AllianceGenome HGNC:16379
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000379965.8 hg38 chr11 5,689,790 5,710,863 21,074
ENST00000454828.6 hg38 chr11 5,689,880 5,710,845 20,966
ENST00000379965.8 hg19 chr11 5,711,020 5,732,093 21,074
ENST00000454828.6 hg19 chr11 5,711,110 5,732,075 20,966
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