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FLJ33534 (uncharacterized LOC285150)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 285150
Atlas_Id 63458
Location 2p25.1  [Link to chromosome band 2p25]
Location_base_pair Starts at 11239126 and ends at 11272347 bp from pter ( according to hg19-Feb_2009)

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)FLJ33534  285150  uncharacterized LOC285150
Aliases
GeneCards (Weizmann)FLJ33534
Ensembl hg19 (Hinxton)ENSG00000145063 [Gene_View]  chr2:11239126-11272347 [Contig_View]  FLJ33534 [Vega]
Ensembl hg38 (Hinxton)ENSG00000145063 [Gene_View]  chr2:11239126-11272347 [Contig_View]  FLJ33534 [Vega]
ICGC DataPortalENSG00000145063
TCGA cBioPortalFLJ33534
AceView (NCBI)FLJ33534
Genatlas (Paris)FLJ33534
WikiGenes285150
SOURCE (Princeton)FLJ33534
Genetics Home Reference (NIH)FLJ33534
Genomic and cartography
GoldenPath hg19 (UCSC)FLJ33534  -     chr2:11239126-11272347 -  2p25.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)FLJ33534  -     2p25.1   [Description]    (hg38-Dec_2013)
EnsemblFLJ33534 - 2p25.1 [CytoView hg19]  FLJ33534 - 2p25.1 [CytoView hg38]
Mapping of homologs : NCBIFLJ33534 [Mapview hg19]  FLJ33534 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK090853 AK311163 BC111723 HG493649 HG493650
RefSeq transcript (Entrez)NM_182586
RefSeq genomic (Entrez)NC_000002 NC_018913 NT_005334 NW_004929298
Consensus coding sequences : CCDS (NCBI)FLJ33534
Cluster EST : UnigeneHs.329841 [ NCBI ]
CGAP (NCI)Hs.329841
Alternative Splicing GalleryENSG00000145063
Gene ExpressionFLJ33534 [ NCBI-GEO ]   FLJ33534 [ EBI - ARRAY_EXPRESS ]   FLJ33534 [ SEEK ]   FLJ33534 [ MEM ]
Gene Expression Viewer (FireBrowse)FLJ33534 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)285150
GTEX Portal (Tissue expression)FLJ33534
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N2B8   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N2B8  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N2B8
Splice isoforms : SwissVarQ8N2B8
PhosPhoSitePlusQ8N2B8
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)FLJ33534
DMDM Disease mutations285150
Blocks (Seattle)FLJ33534
SuperfamilyQ8N2B8
Human Protein AtlasENSG00000145063
Peptide AtlasQ8N2B8
HPRD08158
IPIIPI00166369   IPI00872244   
Protein Interaction databases
DIP (DOE-UCLA)Q8N2B8
IntAct (EBI)Q8N2B8
FunCoupENSG00000145063
BioGRIDFLJ33534
STRING (EMBL)FLJ33534
ZODIACFLJ33534
Ontologies - Pathways
QuickGOQ8N2B8
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkFLJ33534
Atlas of Cancer Signalling NetworkFLJ33534
Wikipedia pathwaysFLJ33534
Orthology - Evolution
OrthoDB285150
GeneTree (enSembl)ENSG00000145063
Phylogenetic Trees/Animal Genes : TreeFam-
HOVERGENQ8N2B8
HOGENOMQ8N2B8
Homologs : HomoloGeneFLJ33534
Homology/Alignments : Family Browser (UCSC)FLJ33534
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerFLJ33534 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)FLJ33534
dbVarFLJ33534
ClinVarFLJ33534
1000_GenomesFLJ33534 
Exome Variant ServerFLJ33534
ExAC (Exome Aggregation Consortium)FLJ33534 (select the gene name)
Genetic variants : HAPMAP285150
Genomic Variants (DGV)FLJ33534 [DGVbeta]
DECIPHER (Syndromes)2:11239126-11272347  ENSG00000145063
CONAN: Copy Number AnalysisFLJ33534 
Mutations
ICGC Data Portal- 
TCGA Data Portal- 
Broad Tumor Portal-
OASIS Portal- [ Somatic mutations - Copy number]
Mutations and Diseases : HGMD-
BioMutasearch FLJ33534
DgiDB (Drug Gene Interaction Database)FLJ33534
DoCM (Curated mutations)FLJ33534 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)FLJ33534 (select a term)
intoGenFLJ33534
Cancer3DFLJ33534(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenFLJ33534
Genetic Testing Registry FLJ33534
NextProtQ8N2B8 [Medical]
TSGene285150
GENETestsFLJ33534
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease285150
BioCentury BCIQFLJ33534
ClinGenFLJ33534
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD285150
Clinical trialFLJ33534
Miscellaneous
canSAR (ICR)FLJ33534 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineFLJ33534
EVEXFLJ33534
GoPubMedFLJ33534
iHOPFLJ33534
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 12:05:00 CET 2017

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