RNF167 ring finger protein 167

Information
Symbol
RNF167
Type
protein-coding
Description
ring finger protein 167
Entrez Gene ID
26001
Genome
hg19
Position
chr17:4,843,563-4,848,517
Genome
hg38
Position
chr17:4,940,268-4,945,222
MIM
610431 OMIM
HGNC
HGNC:24544 HGNC
Ensembl
ENSG00000108523 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Uncertain significance 0 44
Ranking
ClinVar
0
0
0
50
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
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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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 :
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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 5730408C10Rik
SYNONYM LP2254
SYNONYM RING105
MIM 610431 OMIM
HGNC HGNC:24544 HGNC
Ensembl ENSG00000108523 Ensembl
AllianceGenome HGNC:24544
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000576229.5 hg38 chr17 4,940,487 4,945,172 4,686
ENST00000262482.11 hg38 chr17 4,940,268 4,945,222 4,955
ENST00000575111.5 hg38 chr17 4,940,381 4,945,191 4,811
ENST00000572430.5 hg38 chr17 4,940,120 4,945,170 5,051
ENST00000571816.5 hg38 chr17 4,940,008 4,945,191 5,184
ENST00000571816.5 hg19 chr17 4,843,303 4,848,486 5,184
ENST00000572430.5 hg19 chr17 4,843,415 4,848,465 5,051
ENST00000262482.11 hg19 chr17 4,843,563 4,848,517 4,955
ENST00000575111.5 hg19 chr17 4,843,676 4,848,486 4,811
ENST00000576229.5 hg19 chr17 4,843,782 4,848,467 4,686
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