RNF39 ring finger protein 39

Information
Symbol
RNF39
Type
protein-coding
Description
ring finger protein 39
Entrez Gene ID
80352
Genome
hg19
Position
chr6:30,038,047-30,043,546
Genome
hg38
Position
chr6:30,070,270-30,075,769
MIM
607524 OMIM
HGNC
HGNC:18064 HGNC
Ensembl
ENSG00000204618 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
not provided 2 0
Uncertain significance 0 44
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
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 FAP216
SYNONYM HZF
SYNONYM HZFW
SYNONYM LIRF
MIM 607524 OMIM
HGNC HGNC:18064 HGNC
Ensembl ENSG00000204618 Ensembl
AllianceGenome HGNC:18064
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000376751.8 hg38 chr6 30,070,266 30,075,849 5,584
ENST00000244360.8 hg38 chr6 30,070,270 30,075,769 5,500
ENST00000376751.8 hg19 chr6 30,038,043 30,043,626 5,584
ENST00000244360.8 hg19 chr6 30,038,047 30,043,546 5,500
Genome browser