C11orf40 chromosome 11 putative open reading frame 40

Information
Symbol
C11orf40
Type
ncRNA
Description
chromosome 11 putative open reading frame 40
Entrez Gene ID
143501
Genome
hg19
Position
chr11:4,592,653-4,599,050
Genome
hg38
Position
chr11:4,571,423-4,577,820
HGNC
HGNC:23986 HGNC
Ensembl
ENSG00000171987 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 NOV1
HGNC HGNC:23986 HGNC
Ensembl ENSG00000171987 Ensembl
AllianceGenome HGNC:23986
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000668205.1 hg38 chr11 4,571,423 4,577,820 6,398
ENST00000668205.1 hg19 chr11 4,592,653 4,599,050 6,398
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