Atlas of Genetics and Cytogenetics in Oncology and Haematology


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FLJ42969 (uncharacterized LOC441374)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 441374
Atlas_Id 63504
Location 8q22.3  [Link to chromosome band 8q22]
Location_base_pair Starts at 101052054 and ends at 101076251 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)

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)-   -
Cards
Entrez_Gene (NCBI)FLJ42969  441374  uncharacterized LOC441374
Aliases
GeneCards (Weizmann)FLJ42969
Ensembl hg19 (Hinxton)ENSG00000248599 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000248599 [Gene_View]  chr8:101052054-101076251 [Contig_View]  FLJ42969 [Vega]
ICGC DataPortalENSG00000248599
TCGA cBioPortalFLJ42969
AceView (NCBI)FLJ42969
Genatlas (Paris)FLJ42969
WikiGenes441374
SOURCE (Princeton)FLJ42969
Genetics Home Reference (NIH)FLJ42969
Genomic and cartography
GoldenPath hg38 (UCSC)FLJ42969  -     chr8:101052054-101076251 +  8q22.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)FLJ42969  -     8q22.3   [Description]    (hg19-Feb_2009)
EnsemblFLJ42969 - 8q22.3 [CytoView hg19]  FLJ42969 - 8q22.3 [CytoView hg38]
Mapping of homologs : NCBIFLJ42969 [Mapview hg19]  FLJ42969 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK124959
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)FLJ42969
Cluster EST : UnigeneHs.652045 [ NCBI ]
CGAP (NCI)Hs.652045
Alternative Splicing GalleryENSG00000248599
Gene ExpressionFLJ42969 [ NCBI-GEO ]   FLJ42969 [ EBI - ARRAY_EXPRESS ]   FLJ42969 [ SEEK ]   FLJ42969 [ MEM ]
Gene Expression Viewer (FireBrowse)FLJ42969 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)441374
GTEX Portal (Tissue expression)FLJ42969
Human Protein AtlasENSG00000248599-FLJ42969 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FLJ42969
DMDM Disease mutations441374
Blocks (Seattle)FLJ42969
Human Protein Atlas [tissue]ENSG00000248599-FLJ42969 [tissue]
Protein Interaction databases
FunCoupENSG00000248599
BioGRIDFLJ42969
STRING (EMBL)FLJ42969
ZODIACFLJ42969
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease441374
BioCentury BCIQFLJ42969
ClinGenFLJ42969
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD441374
Clinical trialFLJ42969
Miscellaneous
canSAR (ICR)FLJ42969 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineFLJ42969
EVEXFLJ42969
GoPubMedFLJ42969
iHOPFLJ42969
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 21 13:45:40 CET 2017

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