C2orf74 chromosome 2 open reading frame 74

Information
Symbol
C2orf74
Type
protein-coding
Description
chromosome 2 open reading frame 74
Entrez Gene ID
339804
Genome
hg19
Position
chr2:61,389,323-61,391,963
Genome
hg38
Position
chr2:61,162,188-61,164,828
HGNC
HGNC:34439 HGNC
Ensembl
ENSG00000237651 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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:34439 HGNC
Ensembl ENSG00000237651 Ensembl
AllianceGenome HGNC:34439
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000464909.2 hg38 chr2 61,145,108 61,164,809 19,702
ENST00000488469.4 hg38 chr2 61,162,191 61,164,825 2,635
ENST00000426997.5 hg38 chr2 61,145,068 61,164,808 19,741
ENST00000432605.3 hg38 chr2 61,162,188 61,164,828 2,641
ENST00000426997.5 hg19 chr2 61,372,203 61,391,943 19,741
ENST00000464909.2 hg19 chr2 61,372,243 61,391,944 19,702
ENST00000432605.3 hg19 chr2 61,389,323 61,391,963 2,641
ENST00000488469.4 hg19 chr2 61,389,326 61,391,960 2,635
KeyValue
strand+
start61,372,202
Gene SymbolC2orf74
Entrez GeneId339,804
Chr Band2p15
end61,391,963
chrchr2
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