TRIM49D2 tripartite motif containing 49D2

Information
Symbol
TRIM49D2
Type
protein-coding
Description
tripartite motif containing 49D2
Entrez Gene ID
729384
Genome
hg19
Position
chr11:89,657,232-89,666,231
Genome
hg38
Position
chr11:89,924,064-89,933,063
HGNC
HGNC:37217 HGNC
Ensembl
ENSG00000233802 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Ranking
ClinVar
0
0
0
2
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 TRIM48L1
SYNONYM TRIM49D1
SYNONYM TRIM49D2P
SYNONYM TRIM49L
SYNONYM TRIM49L1
HGNC HGNC:37217 HGNC
Ensembl ENSG00000233802 Ensembl
AllianceGenome HGNC:37217
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000623787.3 hg38 chr11 89,924,064 89,933,063 9,000
ENST00000526396.3 hg38 chr11 89,926,762 89,932,937 6,176
ENST00000623787.3 hg19 chr11 89,657,232 89,666,231 9,000
ENST00000526396.3 hg19 chr11 89,659,930 89,666,105 6,176
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