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DRP2 (dystrophin related protein 2)

Identity

Other aliasDRP-2
HGNC (Hugo) DRP2
LocusID (NCBI) 1821
Atlas_Id 62646
Location Xq22.1  [Link to chromosome band Xq22]
Location_base_pair Starts at 101219944 and ends at 101264496 bp from pter ( according to hg38-Dec_2013)

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)DRP2   3032
Cards
Entrez_Gene (NCBI)DRP2  1821  dystrophin related protein 2
AliasesDRP-2
GeneCards (Weizmann)DRP2
Ensembl hg19 (Hinxton)ENSG00000102385 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000102385 [Gene_View]  chrX:101219944-101264496 [Contig_View]  DRP2 [Vega]
ICGC DataPortalENSG00000102385
TCGA cBioPortalDRP2
AceView (NCBI)DRP2
Genatlas (Paris)DRP2
WikiGenes1821
SOURCE (Princeton)DRP2
Genetics Home Reference (NIH)DRP2
Genomic and cartography
GoldenPath hg38 (UCSC)DRP2  -     chrX:101219944-101264496 +  Xq22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)DRP2  -     Xq22.1   [Description]    (hg19-Feb_2009)
EnsemblDRP2 - Xq22.1 [CytoView hg19]  DRP2 - Xq22.1 [CytoView hg38]
Mapping of homologs : NCBIDRP2 [Mapview hg19]  DRP2 [Mapview hg38]
OMIM300052   
Gene and transcription
Genbank (Entrez)AB209305 AK091670 AK289825 AK295843 BC036095
RefSeq transcript (Entrez)NM_001171184 NM_001939
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)DRP2
Cluster EST : UnigeneHs.159291 [ NCBI ]
CGAP (NCI)Hs.159291
Alternative Splicing GalleryENSG00000102385
Gene ExpressionDRP2 [ NCBI-GEO ]   DRP2 [ EBI - ARRAY_EXPRESS ]   DRP2 [ SEEK ]   DRP2 [ MEM ]
Gene Expression Viewer (FireBrowse)DRP2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)1821
GTEX Portal (Tissue expression)DRP2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ13474   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ13474  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ13474
Splice isoforms : SwissVarQ13474
PhosPhoSitePlusQ13474
Domaine pattern : Prosite (Expaxy)WW_DOMAIN_1 (PS01159)    WW_DOMAIN_2 (PS50020)    ZF_ZZ_1 (PS01357)    ZF_ZZ_2 (PS50135)   
Domains : Interpro (EBI)Dystrophin-related_2    EF-hand-dom_pair    EF-hand_dom_typ1    EF-hand_dom_typ2    Spectrin/alpha-actinin    Spectrin_repeat    WW_dom    Znf_ZZ   
Domain families : Pfam (Sanger)EF-hand_2 (PF09068)    EF-hand_3 (PF09069)    Spectrin (PF00435)    WW (PF00397)    ZZ (PF00569)   
Domain families : Pfam (NCBI)pfam09068    pfam09069    pfam00435    pfam00397    pfam00569   
Domain families : Smart (EMBL)SPEC (SM00150)  WW (SM00456)  ZnF_ZZ (SM00291)  
Conserved Domain (NCBI)DRP2
DMDM Disease mutations1821
Blocks (Seattle)DRP2
SuperfamilyQ13474
Human Protein AtlasENSG00000102385
Peptide AtlasQ13474
HPRD02083
IPIIPI00871834   IPI00955015   IPI00889554   
Protein Interaction databases
DIP (DOE-UCLA)Q13474
IntAct (EBI)Q13474
FunCoupENSG00000102385
BioGRIDDRP2
STRING (EMBL)DRP2
ZODIACDRP2
Ontologies - Pathways
QuickGOQ13474
Ontology : AmiGOcentral nervous system development  zinc ion binding  postsynaptic density  cell junction  dendrite  perikaryon  postsynaptic membrane  synapse organization  
Ontology : EGO-EBIcentral nervous system development  zinc ion binding  postsynaptic density  cell junction  dendrite  perikaryon  postsynaptic membrane  synapse organization  
NDEx NetworkDRP2
Atlas of Cancer Signalling NetworkDRP2
Wikipedia pathwaysDRP2
Orthology - Evolution
OrthoDB1821
GeneTree (enSembl)ENSG00000102385
Phylogenetic Trees/Animal Genes : TreeFamDRP2
HOVERGENQ13474
HOGENOMQ13474
Homologs : HomoloGeneDRP2
Homology/Alignments : Family Browser (UCSC)DRP2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerDRP2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)DRP2
dbVarDRP2
ClinVarDRP2
1000_GenomesDRP2 
Exome Variant ServerDRP2
ExAC (Exome Aggregation Consortium)DRP2 (select the gene name)
Genetic variants : HAPMAP1821
Genomic Variants (DGV)DRP2 [DGVbeta]
DECIPHERDRP2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisDRP2 
Mutations
ICGC Data PortalDRP2 
TCGA Data PortalDRP2 
Broad Tumor PortalDRP2
OASIS PortalDRP2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICDRP2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDDRP2
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
LOVD (Leiden Open Variation Database)X-chromosome gene database
BioMutasearch DRP2
DgiDB (Drug Gene Interaction Database)DRP2
DoCM (Curated mutations)DRP2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)DRP2 (select a term)
intoGenDRP2
Cancer3DDRP2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM300052   
Orphanet
MedgenDRP2
Genetic Testing Registry DRP2
NextProtQ13474 [Medical]
TSGene1821
GENETestsDRP2
Target ValidationDRP2
Huge Navigator DRP2 [HugePedia]
snp3D : Map Gene to Disease1821
BioCentury BCIQDRP2
ClinGenDRP2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD1821
Chemical/Pharm GKB GenePA27486
Clinical trialDRP2
Miscellaneous
canSAR (ICR)DRP2 (select the gene name)
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineDRP2
EVEXDRP2
GoPubMedDRP2
iHOPDRP2
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 13:06:40 CEST 2017

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