RNFT2 ring finger protein, transmembrane 2

Information
Symbol
RNFT2
Type
protein-coding
Description
ring finger protein, transmembrane 2
Entrez Gene ID
84900
Genome
hg19
Position
chr12:117,176,120-117,291,436
Genome
hg38
Position
chr12:116,738,315-116,853,631
MIM
620254 OMIM
HGNC
HGNC:25905 HGNC
Ensembl
ENSG00000135119 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 15 0
Uncertain significance 0 50
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 TMEM118
MIM 620254 OMIM
HGNC HGNC:25905 HGNC
Ensembl ENSG00000135119 Ensembl
AllianceGenome HGNC:25905
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000407967.7 hg38 chr12 116,738,291 116,853,631 115,341
ENST00000677328.1 hg38 chr12 116,759,935 116,810,520 50,586
ENST00000392549.7 hg38 chr12 116,738,291 116,852,944 114,654
ENST00000257575.9 hg38 chr12 116,738,315 116,853,631 115,317
ENST00000392549.7 hg19 chr12 117,176,096 117,290,749 114,654
ENST00000407967.7 hg19 chr12 117,176,096 117,291,436 115,341
ENST00000257575.9 hg19 chr12 117,176,120 117,291,436 115,317
ENST00000677328.1 hg19 chr12 117,197,740 117,248,325 50,586
Genome browser