RNF169 ring finger protein 169

Information
Symbol
RNF169
Type
protein-coding
Description
ring finger protein 169
Entrez Gene ID
254225
Genome
hg19
Position
chr11:74,459,894-74,553,458
Genome
hg38
Position
chr11:74,748,849-74,842,413
MIM
618650 OMIM
HGNC
HGNC:26961 HGNC
Ensembl
ENSG00000166439 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 78
Ranking
ClinVar
0
0
0
82
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 618650 OMIM
HGNC HGNC:26961 HGNC
Ensembl ENSG00000166439 Ensembl
AllianceGenome HGNC:26961
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000299563.5 hg38 chr11 74,748,849 74,842,413 93,565
ENST00000299563.5 hg19 chr11 74,459,894 74,553,458 93,565
Genome browser