RNF113B ring finger protein 113B

Information
Symbol
RNF113B
Type
protein-coding
Description
ring finger protein 113B
Entrez Gene ID
140432
Genome
hg19
Position
chr13:98,828,039-98,829,523
Genome
hg38
Position
chr13:98,175,785-98,177,269
HGNC
HGNC:17267 HGNC
Ensembl
ENSG00000139797 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
50
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 :
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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 RNF161
SYNONYM ZNF183L1
SYNONYM bA10G5.1
HGNC HGNC:17267 HGNC
Ensembl ENSG00000139797 Ensembl
AllianceGenome HGNC:17267
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000267291.7 hg38 chr13 98,175,785 98,177,269 1,485
ENST00000267291.7 hg19 chr13 98,828,039 98,829,523 1,485
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