TRIM32 tripartite motif containing 32

Information
Symbol
TRIM32
Type
protein-coding
Description
tripartite motif containing 32
Entrez Gene ID
22954
Genome
hg19
Position
chr9:119,449,584-119,463,578
Genome
hg38
Position
chr9:116,687,305-116,701,299
MIM
602290 OMIM
HGNC
HGNC:16380 HGNC
Ensembl
ENSG00000119401 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 78
Likely pathogenic 1 34
Benign 0 20
Likely benign 0 412
Conflicting classifications of pathogenicity 0 94
not provided 4 0
Uncertain significance 0 682
Ranking
ClinVar
0
0
324
880
4
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 BBS11
SYNONYM HT2A
SYNONYM LGMD2H
SYNONYM LGMDR8
SYNONYM TATIP
MIM 602290 OMIM
HGNC HGNC:16380 HGNC
Ensembl ENSG00000119401 Ensembl
AllianceGenome HGNC:16380
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000373983.2 hg38 chr9 116,687,330 116,701,300 13,971
ENST00000450136.2 hg38 chr9 116,687,305 116,701,299 13,995
ENST00000450136.2 hg19 chr9 119,449,584 119,463,578 13,995
ENST00000373983.2 hg19 chr9 119,449,609 119,463,579 13,971
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