Atlas of Genetics and Cytogenetics in Oncology and Haematology


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CHURC1-FNTB (CHURC1-FNTB readthrough)

Identity

Other alias-
HGNC (Hugo) CHURC1-FNTB
LocusID (NCBI) 100529261
Atlas_Id 61830
Location 14q23.3  [Link to chromosome band 14q23]
Location_base_pair Starts at 64914361 and ends at 65062655 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
CHURC1-FNTB (14q23.3) / CAMSAP2 (1q32.1)SCLY (2q37.3) / CHURC1-FNTB (14q23.3)

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)CHURC1-FNTB   42960
Cards
Entrez_Gene (NCBI)CHURC1-FNTB  100529261  CHURC1-FNTB readthrough
Aliases
GeneCards (Weizmann)CHURC1-FNTB
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr14:64914361-65062655 [Contig_View]  CHURC1-FNTB [Vega]
TCGA cBioPortalCHURC1-FNTB
AceView (NCBI)CHURC1-FNTB
Genatlas (Paris)CHURC1-FNTB
WikiGenes100529261
SOURCE (Princeton)CHURC1-FNTB
Genetics Home Reference (NIH)CHURC1-FNTB
Genomic and cartography
GoldenPath hg38 (UCSC)CHURC1-FNTB  -     chr14:64914361-65062655 +  14q23.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)CHURC1-FNTB  -     14q23.3   [Description]    (hg19-Feb_2009)
EnsemblCHURC1-FNTB - 14q23.3 [CytoView hg19]  CHURC1-FNTB - 14q23.3 [CytoView hg38]
Mapping of homologs : NCBICHURC1-FNTB [Mapview hg19]  CHURC1-FNTB [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK296850 AK303739
RefSeq transcript (Entrez)NM_001202558 NM_001202559
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)CHURC1-FNTB
Cluster EST : UnigeneHs.325531 [ NCBI ]
CGAP (NCI)Hs.325531
Gene ExpressionCHURC1-FNTB [ NCBI-GEO ]   CHURC1-FNTB [ EBI - ARRAY_EXPRESS ]   CHURC1-FNTB [ SEEK ]   CHURC1-FNTB [ MEM ]
Gene Expression Viewer (FireBrowse)CHURC1-FNTB [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100529261
GTEX Portal (Tissue expression)CHURC1-FNTB
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)CHURC1-FNTB
DMDM Disease mutations100529261
Blocks (Seattle)CHURC1-FNTB
IPIIPI01011588   IPI00909112   IPI00984229   
Protein Interaction databases
BioGRIDCHURC1-FNTB
STRING (EMBL)CHURC1-FNTB
ZODIACCHURC1-FNTB
Ontologies - Pathways
Huge Navigator CHURC1-FNTB [HugePedia]
snp3D : Map Gene to Disease100529261
BioCentury BCIQCHURC1-FNTB
ClinGenCHURC1-FNTB
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100529261
Clinical trialCHURC1-FNTB
Miscellaneous
canSAR (ICR)CHURC1-FNTB (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineCHURC1-FNTB
EVEXCHURC1-FNTB
GoPubMedCHURC1-FNTB
iHOPCHURC1-FNTB
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Nov 21 13:29:20 CET 2017

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