C22orf42 chromosome 22 open reading frame 42

Information
Symbol
C22orf42
Type
protein-coding
Description
chromosome 22 open reading frame 42
Entrez Gene ID
150297
Genome
hg19
Position
chr22:32,544,993-32,555,290
Genome
hg38
Position
chr22:32,149,006-32,159,303
HGNC
HGNC:27160 HGNC
Ensembl
ENSG00000205856 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 4
Ranking
ClinVar
0
0
0
4
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 dJ90G24.6
HGNC HGNC:27160 HGNC
Ensembl ENSG00000205856 Ensembl
AllianceGenome HGNC:27160
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000382097.4 hg38 chr22 32,149,006 32,159,303 10,298
ENST00000382097.4 hg19 chr22 32,544,993 32,555,290 10,298
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