C11orf16 chromosome 11 open reading frame 16

Information
Symbol
C11orf16
Type
protein-coding
Description
chromosome 11 open reading frame 16
Entrez Gene ID
56673
Genome
hg19
Position
chr11:8,941,623-8,954,494
Genome
hg38
Position
chr11:8,920,076-8,932,947
HGNC
HGNC:1169 HGNC
Ensembl
ENSG00000176029 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 8
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:1169 HGNC
Ensembl ENSG00000176029 Ensembl
AllianceGenome HGNC:1169
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000326053.10 hg38 chr11 8,920,076 8,932,947 12,872
ENST00000525780.5 hg38 chr11 8,920,076 8,932,988 12,913
ENST00000326053.10 hg19 chr11 8,941,623 8,954,494 12,872
ENST00000525780.5 hg19 chr11 8,941,623 8,954,535 12,913
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