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DPCD (deleted in primary ciliary dyskinesia homolog (mouse))

Identity

Alias (NCBI)-
HGNC (Hugo) DPCD
HGNC Alias symbDKFZP566F084
RP11-529I10.4
LocusID (NCBI) 25911
Atlas_Id 62601
Location 10q24.32  [Link to chromosome band 10q24]
Location_base_pair Starts at 101588321 and ends at 101609662 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
DOCK1 (10q26.2) / DPCD (10q24.32)PMEL (12q13.2) / DPCD (10q24.32)

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)DPCD   24542
Cards
Entrez_Gene (NCBI)DPCD    deleted in primary ciliary dyskinesia homolog (mouse)
Aliases
GeneCards (Weizmann)DPCD
Ensembl hg19 (Hinxton)ENSG00000166171 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000166171 [Gene_View]  ENSG00000166171 [Sequence]  chr10:101588321-101609662 [Contig_View]  DPCD [Vega]
ICGC DataPortalENSG00000166171
TCGA cBioPortalDPCD
AceView (NCBI)DPCD
Genatlas (Paris)DPCD
SOURCE (Princeton)DPCD
Genetics Home Reference (NIH)DPCD
Genomic and cartography
GoldenPath hg38 (UCSC)DPCD  -     chr10:101588321-101609662 +  10q24.32   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)DPCD  -     10q24.32   [Description]    (hg19-Feb_2009)
GoldenPathDPCD - 10q24.32 [CytoView hg19]  DPCD - 10q24.32 [CytoView hg38]
ImmunoBaseENSG00000166171
Genome Data Viewer NCBIDPCD [Mapview hg19]  
OMIM616467   
Gene and transcription
Genbank (Entrez)AK290154 AK296220 AL110240 AY532267 BC001082
RefSeq transcript (Entrez)NM_001329742 NM_001329743 NM_001329744 NM_001329745 NM_001329746 NM_015448
Consensus coding sequences : CCDS (NCBI)DPCD
Gene ExpressionDPCD [ NCBI-GEO ]   DPCD [ EBI - ARRAY_EXPRESS ]   DPCD [ SEEK ]   DPCD [ MEM ]
Gene Expression Viewer (FireBrowse)DPCD [ Firebrowse - Broad ]
GenevisibleExpression of DPCD in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)25911
GTEX Portal (Tissue expression)DPCD
Human Protein AtlasENSG00000166171-DPCD [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9BVM2   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9BVM2  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9BVM2
PhosPhoSitePlusQ9BVM2
Domains : Interpro (EBI)DPCD   
Domain families : Pfam (Sanger)DPCD (PF14913)   
Domain families : Pfam (NCBI)pfam14913   
Conserved Domain (NCBI)DPCD
SuperfamilyQ9BVM2
AlphaFold pdb e-kbQ9BVM2   
Human Protein Atlas [tissue]ENSG00000166171-DPCD [tissue]
HPRD13247
Protein Interaction databases
DIP (DOE-UCLA)Q9BVM2
IntAct (EBI)Q9BVM2
BioGRIDDPCD
STRING (EMBL)DPCD
ZODIACDPCD
Ontologies - Pathways
QuickGOQ9BVM2
Ontology : AmiGOepithelial cilium movement involved in extracellular fluid movement  protein binding  extracellular region  nucleus  spermatogenesis  determination of left/right symmetry  lateral ventricle development  third ventricle development  flagellated sperm motility  left/right pattern formation  
Ontology : EGO-EBIepithelial cilium movement involved in extracellular fluid movement  protein binding  extracellular region  nucleus  spermatogenesis  determination of left/right symmetry  lateral ventricle development  third ventricle development  flagellated sperm motility  left/right pattern formation  
NDEx NetworkDPCD
Atlas of Cancer Signalling NetworkDPCD
Wikipedia pathwaysDPCD
Orthology - Evolution
OrthoDB25911
GeneTree (enSembl)ENSG00000166171
Phylogenetic Trees/Animal Genes : TreeFamDPCD
Homologs : HomoloGeneDPCD
Homology/Alignments : Family Browser (UCSC)DPCD
Gene fusions - Rearrangements
Fusion : QuiverDPCD
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerDPCD [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)DPCD
dbVarDPCD
ClinVarDPCD
MonarchDPCD
1000_GenomesDPCD 
Exome Variant ServerDPCD
GNOMAD BrowserENSG00000166171
Varsome BrowserDPCD
ACMGDPCD variants
VarityQ9BVM2
Genomic Variants (DGV)DPCD [DGVbeta]
DECIPHERDPCD [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisDPCD 
Mutations
ICGC Data PortalDPCD 
TCGA Data PortalDPCD 
Broad Tumor PortalDPCD
OASIS PortalDPCD [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICDPCD  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DDPCD
Mutations and Diseases : HGMDDPCD
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaDPCD
DgiDB (Drug Gene Interaction Database)DPCD
DoCM (Curated mutations)DPCD
CIViC (Clinical Interpretations of Variants in Cancer)DPCD
Cancer3DDPCD
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM616467   
Orphanet
DisGeNETDPCD
MedgenDPCD
Genetic Testing Registry DPCD
NextProtQ9BVM2 [Medical]
GENETestsDPCD
Target ValidationDPCD
Huge Navigator DPCD [HugePedia]
ClinGenDPCD
Clinical trials, drugs, therapy
MyCancerGenomeDPCD
Protein Interactions : CTDDPCD
Pharm GKB GenePA165548502
PharosQ9BVM2
Clinical trialDPCD
Miscellaneous
canSAR (ICR)DPCD
HarmonizomeDPCD
DataMed IndexDPCD
Probes
Litterature
PubMed25 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXDPCD
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:48:17 CEST 2021

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