Atlas of Genetics and Cytogenetics in Oncology and Haematology


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C11orf98 (chromosome 11 open reading frame 98)

Identity

Alias_namesC11orf48
Other alias
HGNC (Hugo) C11orf98
LocusID (NCBI) 102288414
Atlas_Id 60907
Location 11q12.3  [Link to chromosome band 11q12]
Location_base_pair Starts at 62430289 and ends at 62432688 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
C11orf98 (11q12.3) / C11orf98 (11q12.3)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)C11orf98   51238
Cards
Entrez_Gene (NCBI)C11orf98  102288414  chromosome 11 open reading frame 98
AliasesC11orf48
GeneCards (Weizmann)C11orf98
Ensembl hg19 (Hinxton)ENSG00000278615 [Gene_View]  chr11:62430289-62432688 [Contig_View]  C11orf98 [Vega]
Ensembl hg38 (Hinxton)ENSG00000278615 [Gene_View]  chr11:62430289-62432688 [Contig_View]  C11orf98 [Vega]
ICGC DataPortalENSG00000278615
TCGA cBioPortalC11orf98
AceView (NCBI)C11orf98
Genatlas (Paris)C11orf98
WikiGenes102288414
SOURCE (Princeton)C11orf98
Genetics Home Reference (NIH)C11orf98
Genomic and cartography
GoldenPath hg19 (UCSC)C11orf98  -     chr11:62430289-62432688 -  11q12.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)C11orf98  -     11q12.3   [Description]    (hg38-Dec_2013)
EnsemblC11orf98 - 11q12.3 [CytoView hg19]  C11orf98 - 11q12.3 [CytoView hg38]
Mapping of homologs : NCBIC11orf98 [Mapview hg19]  C11orf98 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BF207356 BG563566 BG681685 BQ231052 BX107288
RefSeq transcript (Entrez)NM_001286086
RefSeq genomic (Entrez)NC_000011 NC_018922 NT_167190 NW_004929380
Consensus coding sequences : CCDS (NCBI)C11orf98
Cluster EST : UnigeneHs.9061 [ NCBI ]
CGAP (NCI)Hs.9061
Alternative Splicing GalleryENSG00000278615
Gene ExpressionC11orf98 [ NCBI-GEO ]   C11orf98 [ EBI - ARRAY_EXPRESS ]   C11orf98 [ SEEK ]   C11orf98 [ MEM ]
Gene Expression Viewer (FireBrowse)C11orf98 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102288414
GTEX Portal (Tissue expression)C11orf98
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)C11orf98
DMDM Disease mutations102288414
Blocks (Seattle)C11orf98
Human Protein AtlasENSG00000278615
Protein Interaction databases
FunCoupENSG00000278615
BioGRIDC11orf98
STRING (EMBL)C11orf98
ZODIACC11orf98
Ontologies - Pathways
Huge Navigator C11orf98 [HugePedia]
snp3D : Map Gene to Disease102288414
BioCentury BCIQC11orf98
ClinGenC11orf98
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102288414
Clinical trialC11orf98
Miscellaneous
canSAR (ICR)C11orf98 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineC11orf98
EVEXC11orf98
GoPubMedC11orf98
iHOPC11orf98
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 11:56:24 CET 2017

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