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DLEU7 (deleted in lymphocytic leukemia, 7)

Identity

Alias_symbol (synonym)FLJ44882
Other alias-
HGNC (Hugo) DLEU7
LocusID (NCBI) 220107
Atlas_Id 40332
Location 13q14.3  [Link to chromosome band 13q14]
Location_base_pair Starts at 51397041 and ends at 51418075 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

 


Other Leukemias implicated (Data extracted from papers in the Atlas) [ 1 ]
  del(13q) in chronic lymphocytic leukemia


External links

Nomenclature
HGNC (Hugo)DLEU7   17567
Cards
Entrez_Gene (NCBI)DLEU7  220107  deleted in lymphocytic leukemia, 7
Aliases
GeneCards (Weizmann)DLEU7
Ensembl hg19 (Hinxton)ENSG00000186047 [Gene_View]  chr13:51397041-51418075 [Contig_View]  DLEU7 [Vega]
Ensembl hg38 (Hinxton)ENSG00000186047 [Gene_View]  chr13:51397041-51418075 [Contig_View]  DLEU7 [Vega]
ICGC DataPortalENSG00000186047
TCGA cBioPortalDLEU7
AceView (NCBI)DLEU7
Genatlas (Paris)DLEU7
WikiGenes220107
SOURCE (Princeton)DLEU7
Genetics Home Reference (NIH)DLEU7
Genomic and cartography
GoldenPath hg19 (UCSC)DLEU7  -     chr13:51397041-51418075 -  13q14.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)DLEU7  -     13q14.3   [Description]    (hg38-Dec_2013)
EnsemblDLEU7 - 13q14.3 [CytoView hg19]  DLEU7 - 13q14.3 [CytoView hg38]
Mapping of homologs : NCBIDLEU7 [Mapview hg19]  DLEU7 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK126830 AW024292 AW290996 AY357595 BC104892
RefSeq transcript (Entrez)NM_001306135 NM_198989
RefSeq genomic (Entrez)NC_000013 NC_018924 NT_024524 NW_004929388
Consensus coding sequences : CCDS (NCBI)DLEU7
Cluster EST : UnigeneHs.710878 [ NCBI ]
CGAP (NCI)Hs.710878
Alternative Splicing GalleryENSG00000186047
Gene ExpressionDLEU7 [ NCBI-GEO ]   DLEU7 [ EBI - ARRAY_EXPRESS ]   DLEU7 [ SEEK ]   DLEU7 [ MEM ]
Gene Expression Viewer (FireBrowse)DLEU7 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)220107
GTEX Portal (Tissue expression)DLEU7
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6UYE1   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6UYE1  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6UYE1
Splice isoforms : SwissVarQ6UYE1
PhosPhoSitePlusQ6UYE1
Domains : Interpro (EBI)DLEU7   
Domain families : Pfam (Sanger)DLEU7 (PF15760)   
Domain families : Pfam (NCBI)pfam15760   
Conserved Domain (NCBI)DLEU7
DMDM Disease mutations220107
Blocks (Seattle)DLEU7
SuperfamilyQ6UYE1
Human Protein AtlasENSG00000186047
Peptide AtlasQ6UYE1
HPRD16825
IPIIPI00419798   IPI00844094   IPI00922146   
Protein Interaction databases
DIP (DOE-UCLA)Q6UYE1
IntAct (EBI)Q6UYE1
FunCoupENSG00000186047
BioGRIDDLEU7
STRING (EMBL)DLEU7
ZODIACDLEU7
Ontologies - Pathways
QuickGOQ6UYE1
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkDLEU7
Atlas of Cancer Signalling NetworkDLEU7
Wikipedia pathwaysDLEU7
Orthology - Evolution
OrthoDB220107
GeneTree (enSembl)ENSG00000186047
Phylogenetic Trees/Animal Genes : TreeFamDLEU7
HOVERGENQ6UYE1
HOGENOMQ6UYE1
Homologs : HomoloGeneDLEU7
Homology/Alignments : Family Browser (UCSC)DLEU7
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerDLEU7 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)DLEU7
dbVarDLEU7
ClinVarDLEU7
1000_GenomesDLEU7 
Exome Variant ServerDLEU7
ExAC (Exome Aggregation Consortium)DLEU7 (select the gene name)
Genetic variants : HAPMAP220107
Genomic Variants (DGV)DLEU7 [DGVbeta]
DECIPHER (Syndromes)13:51397041-51418075  ENSG00000186047
CONAN: Copy Number AnalysisDLEU7 
Mutations
ICGC Data PortalDLEU7 
TCGA Data PortalDLEU7 
Broad Tumor PortalDLEU7
OASIS PortalDLEU7 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICDLEU7  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDDLEU7
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch DLEU7
DgiDB (Drug Gene Interaction Database)DLEU7
DoCM (Curated mutations)DLEU7 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)DLEU7 (select a term)
intoGenDLEU7
Cancer3DDLEU7(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenDLEU7
Genetic Testing Registry DLEU7
NextProtQ6UYE1 [Medical]
TSGene220107
GENETestsDLEU7
Huge Navigator DLEU7 [HugePedia]
snp3D : Map Gene to Disease220107
BioCentury BCIQDLEU7
ClinGenDLEU7
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD220107
Chemical/Pharm GKB GenePA142671974
Clinical trialDLEU7
Miscellaneous
canSAR (ICR)DLEU7 (select the gene name)
Probes
Litterature
PubMed16 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineDLEU7
EVEXDLEU7
GoPubMedDLEU7
iHOPDLEU7
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 13:03:23 CET 2017

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