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DRC3 (dynein regulatory complex subunit 3)

Identity

Alias_namesLRRC48
leucine rich repeat containing 48
Alias_symbol (synonym)DKFZP586M1120
CFAP134
Other alias
HGNC (Hugo) DRC3
LocusID (NCBI) 83450
Atlas_Id 77828
Location 17p11.2  [Link to chromosome band 17p11]
Location_base_pair Starts at 17972813 and ends at 18016875 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
ATPAF2 (17p11.2) / DRC3 (17p11.2)SREBF1 (17p11.2) / DRC3 (17p11.2)XPO6 (16p11.2) / DRC3 (17p11.2)

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)DRC3   25384
Cards
Entrez_Gene (NCBI)DRC3  83450  dynein regulatory complex subunit 3
AliasesCFAP134; LRRC48
GeneCards (Weizmann)DRC3
Ensembl hg19 (Hinxton)ENSG00000171962 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000171962 [Gene_View]  chr17:17972813-18016875 [Contig_View]  DRC3 [Vega]
ICGC DataPortalENSG00000171962
TCGA cBioPortalDRC3
AceView (NCBI)DRC3
Genatlas (Paris)DRC3
WikiGenes83450
SOURCE (Princeton)DRC3
Genetics Home Reference (NIH)DRC3
Genomic and cartography
GoldenPath hg38 (UCSC)DRC3  -     chr17:17972813-18016875 +  17p11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)DRC3  -     17p11.2   [Description]    (hg19-Feb_2009)
EnsemblDRC3 - 17p11.2 [CytoView hg19]  DRC3 - 17p11.2 [CytoView hg38]
Mapping of homologs : NCBIDRC3 [Mapview hg19]  DRC3 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK093317 AK293011 AL136926 AM392733 AM392765
RefSeq transcript (Entrez)NM_001130090 NM_001130091 NM_001130092 NM_031294
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)DRC3
Cluster EST : UnigeneHs.579264 [ NCBI ]
CGAP (NCI)Hs.579264
Alternative Splicing GalleryENSG00000171962
Gene ExpressionDRC3 [ NCBI-GEO ]   DRC3 [ EBI - ARRAY_EXPRESS ]   DRC3 [ SEEK ]   DRC3 [ MEM ]
Gene Expression Viewer (FireBrowse)DRC3 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)83450
GTEX Portal (Tissue expression)DRC3
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9H069   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9H069  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9H069
Splice isoforms : SwissVarQ9H069
PhosPhoSitePlusQ9H069
Domaine pattern : Prosite (Expaxy)LRR (PS51450)   
Domains : Interpro (EBI)L_dom-like    Leu-rich_rpt   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)DRC3
DMDM Disease mutations83450
Blocks (Seattle)DRC3
SuperfamilyQ9H069
Human Protein AtlasENSG00000171962
Peptide AtlasQ9H069
HPRD13181
IPIIPI00337516   IPI00737755   
Protein Interaction databases
DIP (DOE-UCLA)Q9H069
IntAct (EBI)Q9H069
FunCoupENSG00000171962
BioGRIDDRC3
STRING (EMBL)DRC3
ZODIACDRC3
Ontologies - Pathways
QuickGOQ9H069
Ontology : AmiGOcytoplasm  axoneme  
Ontology : EGO-EBIcytoplasm  axoneme  
NDEx NetworkDRC3
Atlas of Cancer Signalling NetworkDRC3
Wikipedia pathwaysDRC3
Orthology - Evolution
OrthoDB83450
GeneTree (enSembl)ENSG00000171962
Phylogenetic Trees/Animal Genes : TreeFamDRC3
HOVERGENQ9H069
HOGENOMQ9H069
Homologs : HomoloGeneDRC3
Homology/Alignments : Family Browser (UCSC)DRC3
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerDRC3 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)DRC3
dbVarDRC3
ClinVarDRC3
1000_GenomesDRC3 
Exome Variant ServerDRC3
ExAC (Exome Aggregation Consortium)DRC3 (select the gene name)
Genetic variants : HAPMAP83450
Genomic Variants (DGV)DRC3 [DGVbeta]
DECIPHERDRC3 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisDRC3 
Mutations
ICGC Data PortalDRC3 
TCGA Data PortalDRC3 
Broad Tumor PortalDRC3
OASIS PortalDRC3 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDDRC3
BioMutasearch DRC3
DgiDB (Drug Gene Interaction Database)DRC3
DoCM (Curated mutations)DRC3 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)DRC3 (select a term)
intoGenDRC3
Cancer3DDRC3(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenDRC3
Genetic Testing Registry DRC3
NextProtQ9H069 [Medical]
TSGene83450
GENETestsDRC3
Target ValidationDRC3
Huge Navigator DRC3 [HugePedia]
snp3D : Map Gene to Disease83450
BioCentury BCIQDRC3
ClinGenDRC3
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD83450
Chemical/Pharm GKB GenePA142671508
Clinical trialDRC3
Miscellaneous
canSAR (ICR)DRC3 (select the gene name)
Probes
Litterature
PubMed15 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineDRC3
EVEXDRC3
GoPubMedDRC3
iHOPDRC3
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed Jun 7 15:46:29 CEST 2017

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