RNF128 ring finger protein 128

Information
Symbol
RNF128
Type
protein-coding
Description
ring finger protein 128
Entrez Gene ID
79589
Genome
hg19
Position
chrX:105,969,931-106,040,246
Genome
hg38
Position
chrX:106,726,701-106,797,016
MIM
300439 OMIM
HGNC
HGNC:21153 HGNC
Ensembl
ENSG00000133135 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 12
not provided 6 0
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
64
2
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 :
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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 GRAIL
MIM 300439 OMIM
HGNC HGNC:21153 HGNC
Ensembl ENSG00000133135 Ensembl
AllianceGenome HGNC:21153
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000255499.3 hg38 chrX 106,726,701 106,797,016 70,316
ENST00000324342.7 hg38 chrX 106,693,838 106,796,993 103,156
ENST00000324342.7 hg19 chrX 105,937,068 106,040,223 103,156
ENST00000255499.3 hg19 chrX 105,969,931 106,040,246 70,316
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