RNF121 ring finger protein 121

Information
Symbol
RNF121
Type
protein-coding
Description
ring finger protein 121
Entrez Gene ID
55298
Genome
hg19
Position
chr11:71,640,092-71,708,643
Genome
hg38
Position
chr11:71,929,046-71,997,597
MIM
620529 OMIM
HGNC
HGNC:21070 HGNC
Ensembl
ENSG00000137522 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 28
Ranking
ClinVar
0
0
0
30
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
MIM 620529 OMIM
HGNC HGNC:21070 HGNC
Ensembl ENSG00000137522 Ensembl
AllianceGenome HGNC:21070
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000530137.1 hg38 chr11 71,929,082 71,997,591 68,510
ENST00000393713.7 hg38 chr11 71,929,034 71,997,597 68,564
ENST00000533380.5 hg38 chr11 71,929,032 71,996,593 67,562
ENST00000361756.8 hg38 chr11 71,929,046 71,997,597 68,552
ENST00000533380.5 hg19 chr11 71,640,078 71,707,639 67,562
ENST00000393713.7 hg19 chr11 71,640,080 71,708,643 68,564
ENST00000361756.8 hg19 chr11 71,640,092 71,708,643 68,552
ENST00000530137.1 hg19 chr11 71,640,128 71,708,637 68,510
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