C22orf23 chromosome 22 open reading frame 23

Information
Symbol
C22orf23
Type
protein-coding
Description
chromosome 22 open reading frame 23
Entrez Gene ID
84645
Genome
hg19
Position
chr22:38,339,057-38,349,608
Genome
hg38
Position
chr22:37,943,050-37,953,601
MIM
619678 OMIM
HGNC
HGNC:18589 HGNC
Ensembl
ENSG00000128346 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 2
Ranking
ClinVar
0
0
0
2
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
SYNONYM EVG1
SYNONYM dJ1039K5.6
MIM 619678 OMIM
HGNC HGNC:18589 HGNC
Ensembl ENSG00000128346 Ensembl
AllianceGenome HGNC:18589
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000403026.5 hg38 chr22 37,944,125 37,953,669 9,545
ENST00000403305.6 hg38 chr22 37,943,050 37,953,601 10,552
ENST00000619227.4 hg38 chr22 37,943,050 37,953,669 10,620
ENST00000249079.6 hg38 chr22 37,943,526 37,953,596 10,071
ENST00000403305.6 hg19 chr22 38,339,057 38,349,608 10,552
ENST00000619227.4 hg19 chr22 38,339,057 38,349,676 10,620
ENST00000249079.6 hg19 chr22 38,339,533 38,349,603 10,071
ENST00000403026.5 hg19 chr22 38,340,132 38,349,676 9,545
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