C18orf21 chromosome 18 open reading frame 21

Information
Symbol
C18orf21
Type
protein-coding
Description
chromosome 18 open reading frame 21
Entrez Gene ID
83608
Genome
hg19
Position
chr18:33,552,642-33,559,241
Genome
hg38
Position
chr18:35,972,679-35,979,278
HGNC
HGNC:28802 HGNC
Ensembl
ENSG00000141428 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
SYNONYM HsT3108
SYNONYM PNAS-124
SYNONYM PNAS-131
SYNONYM XTP13
HGNC HGNC:28802 HGNC
Ensembl ENSG00000141428 Ensembl
AllianceGenome HGNC:28802
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000610527.4 hg38 chr18 35,972,625 35,979,286 6,662
ENST00000333234.5 hg38 chr18 35,972,785 35,979,278 6,494
ENST00000592875.6 hg38 chr18 35,972,679 35,979,278 6,600
ENST00000618334.1 hg38 chr18 35,972,625 35,979,286 6,662
ENST00000610527.4 hg19 chr18 33,552,588 33,559,249 6,662
ENST00000618334.1 hg19 chr18 33,552,588 33,559,249 6,662
ENST00000592875.6 hg19 chr18 33,552,642 33,559,241 6,600
ENST00000333234.5 hg19 chr18 33,552,748 33,559,241 6,494
Genome browser