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DISP2 (dispatched RND transporter family member 2)

Identity

Alias_namesdispatched homolog 2 (Drosophila)
Alias_symbol (synonym)DISPB
KIAA1742
HsT16908
Other aliasC15orf36
LINC00594
HGNC (Hugo) DISP2
LocusID (NCBI) 85455
Atlas_Id 62491
Location 15q15.1  [Link to chromosome band 15q15]
Location_base_pair Starts at 40358235 and ends at 40371056 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
DISP2 (15q15.1) / PHGR1 (15q15.1)DISP2 (15q15.1) / TMED10 (14q24.3)

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)DISP2   19712
Cards
Entrez_Gene (NCBI)DISP2  85455  dispatched RND transporter family member 2
AliasesC15orf36; DISPB; HsT16908; LINC00594
GeneCards (Weizmann)DISP2
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr15:40358235-40371056 [Contig_View]  DISP2 [Vega]
TCGA cBioPortalDISP2
AceView (NCBI)DISP2
Genatlas (Paris)DISP2
WikiGenes85455
SOURCE (Princeton)DISP2
Genetics Home Reference (NIH)DISP2
Genomic and cartography
GoldenPath hg38 (UCSC)DISP2  -     chr15:40358235-40371056 +  15q15.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)DISP2  -     15q15.1   [Description]    (hg19-Feb_2009)
EnsemblDISP2 - 15q15.1 [CytoView hg19]  DISP2 - 15q15.1 [CytoView hg38]
Mapping of homologs : NCBIDISP2 [Mapview hg19]  DISP2 [Mapview hg38]
OMIM607503   
Gene and transcription
Genbank (Entrez)AB051529 AI278850 AK096153 BC037537 BC151833
RefSeq transcript (Entrez)NM_033510
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)DISP2
Cluster EST : UnigeneHs.525794 [ NCBI ]
CGAP (NCI)Hs.525794
Gene ExpressionDISP2 [ NCBI-GEO ]   DISP2 [ EBI - ARRAY_EXPRESS ]   DISP2 [ SEEK ]   DISP2 [ MEM ]
Gene Expression Viewer (FireBrowse)DISP2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)85455
GTEX Portal (Tissue expression)DISP2
Protein : pattern, domain, 3D structure
UniProt/SwissProtA7MBM2   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA7MBM2  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA7MBM2
Splice isoforms : SwissVarA7MBM2
PhosPhoSitePlusA7MBM2
Domaine pattern : Prosite (Expaxy)SSD (PS50156)   
Domains : Interpro (EBI)SSD   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)DISP2
DMDM Disease mutations85455
Blocks (Seattle)DISP2
SuperfamilyA7MBM2
Peptide AtlasA7MBM2
HPRD06327
IPIIPI00304587   
Protein Interaction databases
DIP (DOE-UCLA)A7MBM2
IntAct (EBI)A7MBM2
BioGRIDDISP2
STRING (EMBL)DISP2
ZODIACDISP2
Ontologies - Pathways
QuickGOA7MBM2
Ontology : AmiGOmolecular_function  cellular_component  plasma membrane  smoothened signaling pathway  integral component of membrane  
Ontology : EGO-EBImolecular_function  cellular_component  plasma membrane  smoothened signaling pathway  integral component of membrane  
NDEx NetworkDISP2
Atlas of Cancer Signalling NetworkDISP2
Wikipedia pathwaysDISP2
Orthology - Evolution
OrthoDB85455
Phylogenetic Trees/Animal Genes : TreeFamDISP2
HOVERGENA7MBM2
HOGENOMA7MBM2
Homologs : HomoloGeneDISP2
Homology/Alignments : Family Browser (UCSC)DISP2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerDISP2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)DISP2
dbVarDISP2
ClinVarDISP2
1000_GenomesDISP2 
Exome Variant ServerDISP2
ExAC (Exome Aggregation Consortium)DISP2 (select the gene name)
Genetic variants : HAPMAP85455
Genomic Variants (DGV)DISP2 [DGVbeta]
DECIPHERDISP2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisDISP2 
Mutations
ICGC Data PortalDISP2 
TCGA Data PortalDISP2 
Broad Tumor PortalDISP2
OASIS PortalDISP2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICDISP2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDDISP2
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 DISP2
DgiDB (Drug Gene Interaction Database)DISP2
DoCM (Curated mutations)DISP2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)DISP2 (select a term)
intoGenDISP2
Cancer3DDISP2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM607503   
Orphanet
MedgenDISP2
Genetic Testing Registry DISP2
NextProtA7MBM2 [Medical]
TSGene85455
GENETestsDISP2
Target ValidationDISP2
Huge Navigator DISP2 [HugePedia]
snp3D : Map Gene to Disease85455
BioCentury BCIQDISP2
ClinGenDISP2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD85455
Chemical/Pharm GKB GenePA134876083
Clinical trialDISP2
Miscellaneous
canSAR (ICR)DISP2 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineDISP2
EVEXDISP2
GoPubMedDISP2
iHOPDISP2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:06:18 CEST 2017

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