RNF113A ring finger protein 113A

Information
Symbol
RNF113A
Type
protein-coding
Description
ring finger protein 113A
Entrez Gene ID
7737
Genome
hg19
Position
chrX:119,004,438-119,005,696
Genome
hg38
Position
chrX:119,870,475-119,871,733
MIM
300951 OMIM
HGNC
HGNC:12974 HGNC
Ensembl
ENSG00000125352 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Likely pathogenic 0 6
Benign 0 6
Likely benign 0 44
Conflicting classifications of pathogenicity 0 2
not provided 6 0
Uncertain significance 0 120
Ranking
ClinVar
0
0
18
154
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 Cwc24
SYNONYM RNF113
SYNONYM TTD5
SYNONYM ZNF183
MIM 300951 OMIM
HGNC HGNC:12974 HGNC
Ensembl ENSG00000125352 Ensembl
AllianceGenome HGNC:12974
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000371442.4 hg38 chrX 119,870,475 119,871,733 1,259
ENST00000371442.4 hg19 chrX 119,004,438 119,005,696 1,259
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