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DOK6 (docking protein 6)

Identity

Alias_namesDOK5L
docking protein 5-like
Alias_symbol (synonym)MGC20785
HsT3226
Other alias
HGNC (Hugo) DOK6
LocusID (NCBI) 220164
Atlas_Id 62595
Location 18q22.2  [Link to chromosome band 18q22]
Location_base_pair Starts at 69401048 and ends at 69849086 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
DOK6 (18q22.2) / CCDC102B (18q22.1)TRAPPC8 (18q12.1) / DOK6 (18q22.2)

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)DOK6   28301
Cards
Entrez_Gene (NCBI)DOK6  220164  docking protein 6
AliasesDOK5L; HsT3226
GeneCards (Weizmann)DOK6
Ensembl hg19 (Hinxton)ENSG00000206052 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000206052 [Gene_View]  chr18:69401048-69849086 [Contig_View]  DOK6 [Vega]
ICGC DataPortalENSG00000206052
TCGA cBioPortalDOK6
AceView (NCBI)DOK6
Genatlas (Paris)DOK6
WikiGenes220164
SOURCE (Princeton)DOK6
Genetics Home Reference (NIH)DOK6
Genomic and cartography
GoldenPath hg38 (UCSC)DOK6  -     chr18:69401048-69849086 +  18q22.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)DOK6  -     18q22.2   [Description]    (hg19-Feb_2009)
EnsemblDOK6 - 18q22.2 [CytoView hg19]  DOK6 - 18q22.2 [CytoView hg38]
Mapping of homologs : NCBIDOK6 [Mapview hg19]  DOK6 [Mapview hg38]
OMIM611402   
Gene and transcription
Genbank (Entrez)AK057795 AL512695 AY599248 BC008583 BC019045
RefSeq transcript (Entrez)NM_152721
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)DOK6
Cluster EST : UnigeneHs.278285 [ NCBI ]
CGAP (NCI)Hs.278285
Alternative Splicing GalleryENSG00000206052
Gene ExpressionDOK6 [ NCBI-GEO ]   DOK6 [ EBI - ARRAY_EXPRESS ]   DOK6 [ SEEK ]   DOK6 [ MEM ]
Gene Expression Viewer (FireBrowse)DOK6 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)220164
GTEX Portal (Tissue expression)DOK6
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6PKX4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6PKX4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6PKX4
Splice isoforms : SwissVarQ6PKX4
PhosPhoSitePlusQ6PKX4
Domaine pattern : Prosite (Expaxy)IRS_PTB (PS51064)   
Domains : Interpro (EBI)IRS_PTB    PH_dom-like    PH_domain   
Domain families : Pfam (Sanger)IRS (PF02174)   
Domain families : Pfam (NCBI)pfam02174   
Domain families : Smart (EMBL)PH (SM00233)  PTBI (SM00310)  
Conserved Domain (NCBI)DOK6
DMDM Disease mutations220164
Blocks (Seattle)DOK6
SuperfamilyQ6PKX4
Human Protein AtlasENSG00000206052
Peptide AtlasQ6PKX4
HPRD13244
IPIIPI00400860   
Protein Interaction databases
DIP (DOE-UCLA)Q6PKX4
IntAct (EBI)Q6PKX4
FunCoupENSG00000206052
BioGRIDDOK6
STRING (EMBL)DOK6
ZODIACDOK6
Ontologies - Pathways
QuickGOQ6PKX4
Ontology : AmiGOinsulin receptor binding  protein binding  cytosol  axon guidance  
Ontology : EGO-EBIinsulin receptor binding  protein binding  cytosol  axon guidance  
NDEx NetworkDOK6
Atlas of Cancer Signalling NetworkDOK6
Wikipedia pathwaysDOK6
Orthology - Evolution
OrthoDB220164
GeneTree (enSembl)ENSG00000206052
Phylogenetic Trees/Animal Genes : TreeFamDOK6
HOVERGENQ6PKX4
HOGENOMQ6PKX4
Homologs : HomoloGeneDOK6
Homology/Alignments : Family Browser (UCSC)DOK6
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerDOK6 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)DOK6
dbVarDOK6
ClinVarDOK6
1000_GenomesDOK6 
Exome Variant ServerDOK6
ExAC (Exome Aggregation Consortium)DOK6 (select the gene name)
Genetic variants : HAPMAP220164
Genomic Variants (DGV)DOK6 [DGVbeta]
DECIPHERDOK6 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisDOK6 
Mutations
ICGC Data PortalDOK6 
TCGA Data PortalDOK6 
Broad Tumor PortalDOK6
OASIS PortalDOK6 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICDOK6  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDDOK6
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 DOK6
DgiDB (Drug Gene Interaction Database)DOK6
DoCM (Curated mutations)DOK6 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)DOK6 (select a term)
intoGenDOK6
Cancer3DDOK6(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM611402   
Orphanet
MedgenDOK6
Genetic Testing Registry DOK6
NextProtQ6PKX4 [Medical]
TSGene220164
GENETestsDOK6
Target ValidationDOK6
Huge Navigator DOK6 [HugePedia]
snp3D : Map Gene to Disease220164
BioCentury BCIQDOK6
ClinGenDOK6
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD220164
Chemical/Pharm GKB GenePA134866995
Clinical trialDOK6
Miscellaneous
canSAR (ICR)DOK6 (select the gene name)
Probes
Litterature
PubMed11 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineDOK6
EVEXDOK6
GoPubMedDOK6
iHOPDOK6
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 15:46:19 CEST 2017

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