C11orf86 chromosome 11 open reading frame 86

Information
Symbol
C11orf86
Type
protein-coding
Description
chromosome 11 open reading frame 86
Entrez Gene ID
254439
Genome
hg19
Position
chr11:66,742,775-66,744,480
Genome
hg38
Position
chr11:66,975,304-66,977,009
HGNC
HGNC:34442 HGNC
Ensembl
ENSG00000173237 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 6
Ranking
ClinVar
0
0
0
6
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 FACI
HGNC HGNC:34442 HGNC
Ensembl ENSG00000173237 Ensembl
AllianceGenome HGNC:34442
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000308963.4 hg38 chr11 66,975,277 66,977,004 1,728
ENST00000683896.1 hg38 chr11 66,975,304 66,977,009 1,706
ENST00000308963.4 hg19 chr11 66,742,748 66,744,475 1,728
ENST00000683896.1 hg19 chr11 66,742,775 66,744,480 1,706
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