C11orf42 chromosome 11 open reading frame 42

Information
Symbol
C11orf42
Type
protein-coding
Description
chromosome 11 open reading frame 42
Entrez Gene ID
160298
Genome
hg19
Position
chr11:6,226,787-6,232,365
Genome
hg38
Position
chr11:6,205,557-6,211,135
HGNC
HGNC:28541 HGNC
Ensembl
ENSG00000180878 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 6
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 :
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
HGNC HGNC:28541 HGNC
Ensembl ENSG00000180878 Ensembl
AllianceGenome HGNC:28541
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000316375.3 hg38 chr11 6,205,557 6,211,135 5,579
ENST00000316375.3 hg19 chr11 6,226,787 6,232,365 5,579
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