C2orf42 chromosome 2 open reading frame 42

Information
Symbol
C2orf42
Type
protein-coding
Description
chromosome 2 open reading frame 42
Entrez Gene ID
54980
Genome
hg19
Position
chr2:70,377,017-70,418,151
Genome
hg38
Position
chr2:70,149,885-70,191,019
HGNC
HGNC:26056 HGNC
Ensembl
ENSG00000115998 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
12
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
HGNC HGNC:26056 HGNC
Ensembl ENSG00000115998 Ensembl
AllianceGenome HGNC:26056
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000264434.7 hg38 chr2 70,149,885 70,191,019 41,135
ENST00000420306.1 hg38 chr2 70,149,898 70,181,995 32,098
ENST00000264434.7 hg19 chr2 70,377,017 70,418,151 41,135
ENST00000420306.1 hg19 chr2 70,377,030 70,409,127 32,098
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