RNF31 ring finger protein 31

Information
Symbol
RNF31
Type
protein-coding
Description
ring finger protein 31
Entrez Gene ID
55072
Genome
hg19
Position
chr14:24,616,707-24,629,864
Genome
hg38
Position
chr14:24,147,498-24,160,655
MIM
612487 OMIM
HGNC
HGNC:16031 HGNC
Ensembl
ENSG00000092098 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 2 4
Likely pathogenic 0 2
Benign 0 48
Likely benign 0 572
Conflicting classifications of pathogenicity 0 16
Uncertain significance 0 672
Ranking
ClinVar
0
0
100
1,186
6
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 HOIP
SYNONYM IMD115
SYNONYM Paul
SYNONYM ZIBRA
MIM 612487 OMIM
HGNC HGNC:16031 HGNC
Ensembl ENSG00000092098 Ensembl
AllianceGenome HGNC:16031
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000559533.6 hg38 chr14 24,146,740 24,160,660 13,921
ENST00000559275.5 hg38 chr14 24,146,887 24,160,659 13,773
ENST00000324103.11 hg38 chr14 24,147,498 24,160,655 13,158
ENST00000699885.1 hg38 chr14 24,147,498 24,160,655 13,158
ENST00000559533.6 hg19 chr14 24,615,949 24,629,869 13,921
ENST00000559275.5 hg19 chr14 24,616,096 24,629,868 13,773
ENST00000324103.11 hg19 chr14 24,616,707 24,629,864 13,158
ENST00000699885.1 hg19 chr14 24,616,707 24,629,864 13,158
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