TRIM29 tripartite motif containing 29

Information
Symbol
TRIM29
Type
protein-coding
Description
tripartite motif containing 29
Entrez Gene ID
23650
Genome
hg19
Position
chr11:119,981,994-120,008,821
Genome
hg38
Position
chr11:120,111,286-120,138,113
MIM
610658 OMIM
HGNC
HGNC:17274 HGNC
Ensembl
ENSG00000137699 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Uncertain significance 0 110
Ranking
ClinVar
0
0
0
114
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 ATDC
MIM 610658 OMIM
HGNC HGNC:17274 HGNC
Ensembl ENSG00000137699 Ensembl
AllianceGenome HGNC:17274
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000529044.5 hg38 chr11 120,112,410 120,128,913 16,504
ENST00000528870.5 hg38 chr11 120,112,410 120,125,578 13,169
ENST00000341846.10 hg38 chr11 120,111,286 120,138,113 26,828
ENST00000627238.1 hg38 chr11 120,137,370 120,138,031 662
ENST00000341846.10 hg19 chr11 119,981,994 120,008,821 26,828
ENST00000528870.5 hg19 chr11 119,983,118 119,996,286 13,169
ENST00000529044.5 hg19 chr11 119,983,118 119,999,621 16,504
ENST00000627238.1 hg19 chr11 120,008,078 120,008,739 662
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