TRIM49 tripartite motif containing 49

Information
Symbol
TRIM49
Type
protein-coding
Description
tripartite motif containing 49
Entrez Gene ID
57093
Genome
hg19
Position
chr11:89,530,823-89,541,743
Genome
hg38
Position
chr11:89,797,655-89,808,575
MIM
606124 OMIM
HGNC
HGNC:13431 HGNC
Ensembl
ENSG00000168930 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
56
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 RNF18
SYNONYM TRIM49A
SYNONYM TRIM49L2
MIM 606124 OMIM
HGNC HGNC:13431 HGNC
Ensembl ENSG00000168930 Ensembl
AllianceGenome HGNC:13431
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000329758.5 hg38 chr11 89,797,655 89,808,575 10,921
ENST00000532501.2 hg38 chr11 89,797,947 89,807,220 9,274
ENST00000329758.5 hg19 chr11 89,530,823 89,541,743 10,921
ENST00000532501.2 hg19 chr11 89,531,115 89,540,388 9,274
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