Atlas of Genetics and Cytogenetics in Oncology and Haematology


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C2orf27B (chromosome 2 open reading frame 27B)

Identity

Alias_symbol (synonym)MGC50273
Other alias-
HGNC (Hugo) C2orf27B
LocusID (NCBI) 408029
Atlas_Id 61151
Location 2q21.2  [Link to chromosome band 2q21]
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)C2orf27B   33824
Cards
Entrez_Gene (NCBI)C2orf27B  408029  chromosome 2 open reading frame 27B
Aliases
GeneCards (Weizmann)C2orf27B
Ensembl hg19 (Hinxton)ENSG00000186825 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000186825 [Gene_View]  ENSG00000186825 [Sequence]  - [Contig_View]  C2orf27B [Vega]
ICGC DataPortalENSG00000186825
TCGA cBioPortalC2orf27B
AceView (NCBI)C2orf27B
Genatlas (Paris)C2orf27B
WikiGenes408029
SOURCE (Princeton)C2orf27B
Genetics Home Reference (NIH)C2orf27B
Genomic and cartography
GoldenPath hg38 (UCSC)C2orf27B  -  
GoldenPath hg19 (UCSC)C2orf27B  -  
GoldenPathC2orf27B - [CytoView hg19]  C2orf27B - [CytoView hg38]
ImmunoBaseENSG00000186825
Mapping of homologs : NCBIC2orf27B [Mapview hg19]  C2orf27B [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC043584 DB334481
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000002 NT_187528
Consensus coding sequences : CCDS (NCBI)C2orf27B
Alternative Splicing GalleryENSG00000186825
Gene ExpressionC2orf27B [ NCBI-GEO ]   C2orf27B [ EBI - ARRAY_EXPRESS ]   C2orf27B [ SEEK ]   C2orf27B [ MEM ]
Gene Expression Viewer (FireBrowse)C2orf27B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)408029
GTEX Portal (Tissue expression)C2orf27B
Human Protein AtlasENSG00000186825-C2orf27B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)C2orf27B
DMDM Disease mutations408029
Blocks (Seattle)C2orf27B
Human Protein Atlas [tissue]ENSG00000186825-C2orf27B [tissue]
HPRD14664
IPIIPI00604591   IPI00384553   IPI00787169   
Protein Interaction databases
FunCoupENSG00000186825
BioGRIDC2orf27B
STRING (EMBL)C2orf27B
ZODIACC2orf27B
Ontologies - Pathways
Huge Navigator C2orf27B [HugePedia]
snp3D : Map Gene to Disease408029
BioCentury BCIQC2orf27B
ClinGenC2orf27B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD408029
Chemical/Pharm GKB GenePA164717134
Clinical trialC2orf27B
Miscellaneous
canSAR (ICR)C2orf27B (select the gene name)
HarmonizomeC2orf27B
DataMed IndexC2orf27B
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineC2orf27B
EVEXC2orf27B
GoPubMedC2orf27B
iHOPC2orf27B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Sun May 10 11:26:34 CEST 2020

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