C11orf58 chromosome 11 open reading frame 58

Information
Symbol
C11orf58
Type
protein-coding
Description
chromosome 11 open reading frame 58
Entrez Gene ID
10944
Genome
hg19
Position
chr11:16,760,194-16,779,887
Genome
hg38
Position
chr11:16,738,647-16,758,340
MIM
619625 OMIM
HGNC
HGNC:16990 HGNC
Ensembl
ENSG00000110696 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 IMAGE145052
SYNONYM SMAP
MIM 619625 OMIM
HGNC HGNC:16990 HGNC
Ensembl ENSG00000110696 Ensembl
AllianceGenome HGNC:16990
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000228136.9 hg38 chr11 16,738,647 16,758,340 19,694
ENST00000528634.5 hg38 chr11 16,738,658 16,755,055 16,398
ENST00000525684.1 hg38 chr11 16,738,658 16,755,067 16,410
ENST00000228136.9 hg19 chr11 16,760,194 16,779,887 19,694
ENST00000528634.5 hg19 chr11 16,760,205 16,776,602 16,398
ENST00000525684.1 hg19 chr11 16,760,205 16,776,614 16,410
Genome browser