C22orf39 chromosome 22 open reading frame 39

Information
Symbol
C22orf39
Type
protein-coding
Description
chromosome 22 open reading frame 39
Entrez Gene ID
128977
Genome
hg19
Position
chr22:19,428,409-19,435,234
Genome
hg38
Position
chr22:19,440,886-19,447,711
HGNC
HGNC:27012 HGNC
Ensembl
ENSG00000242259 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 14 0
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
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 Pants
HGNC HGNC:27012 HGNC
Ensembl ENSG00000242259 Ensembl
AllianceGenome HGNC:27012
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000399568.5 hg38 chr22 19,440,886 19,447,692 6,807
ENST00000399562.9 hg38 chr22 19,440,886 19,447,711 6,826
ENST00000399568.5 hg19 chr22 19,428,409 19,435,215 6,807
ENST00000399562.9 hg19 chr22 19,428,409 19,435,234 6,826
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