C11orf24 chromosome 11 open reading frame 24

Information
Symbol
C11orf24
Type
protein-coding
Description
chromosome 11 open reading frame 24
Entrez Gene ID
53838
Genome
hg19
Position
chr11:68,028,806-68,039,441
Genome
hg38
Position
chr11:68,261,338-68,271,973
MIM
610880 OMIM
HGNC
HGNC:1174 HGNC
Ensembl
ENSG00000171067 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 2
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
SYNONYM DM4E3
MIM 610880 OMIM
HGNC HGNC:1174 HGNC
Ensembl ENSG00000171067 Ensembl
AllianceGenome HGNC:1174
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000533310.5 hg38 chr11 68,261,609 68,271,947 10,339
ENST00000304271.11 hg38 chr11 68,261,338 68,271,973 10,636
ENST00000304271.11 hg19 chr11 68,028,806 68,039,441 10,636
ENST00000533310.5 hg19 chr11 68,029,077 68,039,415 10,339
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