C2orf80 chromosome 2 open reading frame 80

Information
Symbol
C2orf80
Type
protein-coding
Description
chromosome 2 open reading frame 80
Entrez Gene ID
389073
Genome
hg19
Position
chr2:209,030,071-209,054,754
Genome
hg38
Position
chr2:208,165,347-208,190,030
MIM
615536 OMIM
HGNC
HGNC:34352 HGNC
Ensembl
ENSG00000188674 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
8
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 :
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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 :
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 GONDA1
MIM 615536 OMIM
HGNC HGNC:34352 HGNC
Ensembl ENSG00000188674 Ensembl
AllianceGenome HGNC:34352
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000341287.9 hg38 chr2 208,165,347 208,190,030 24,684
ENST00000451346.5 hg38 chr2 208,165,355 208,190,024 24,670
ENST00000453017.5 hg38 chr2 208,165,478 208,187,004 21,527
ENST00000341287.9 hg19 chr2 209,030,071 209,054,754 24,684
ENST00000451346.5 hg19 chr2 209,030,079 209,054,748 24,670
ENST00000453017.5 hg19 chr2 209,030,202 209,051,728 21,527
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