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CEP295NL (CEP295 N-terminal like)

Identity

Alias_namesKIAA1731NL
KIAA1731 N-terminal like
Alias_symbol (synonym)DDC8
Other alias
HGNC (Hugo) CEP295NL
LocusID (NCBI) 100653515
Atlas_Id 76807
Location 17q25.3  [Link to chromosome band 17q25]
Location_base_pair Starts at 78890580 and ends at 78903217 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)CEP295NL   44659
Cards
Entrez_Gene (NCBI)CEP295NL  100653515  CEP295 N-terminal like
AliasesDDC8; KIAA1731NL
GeneCards (Weizmann)CEP295NL
Ensembl hg19 (Hinxton)ENSG00000178404 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000178404 [Gene_View]  chr17:78890580-78903217 [Contig_View]  CEP295NL [Vega]
ICGC DataPortalENSG00000178404
TCGA cBioPortalCEP295NL
AceView (NCBI)CEP295NL
Genatlas (Paris)CEP295NL
WikiGenes100653515
SOURCE (Princeton)CEP295NL
Genetics Home Reference (NIH)CEP295NL
Genomic and cartography
GoldenPath hg38 (UCSC)CEP295NL  -     chr17:78890580-78903217 -  17q25.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)CEP295NL  -     17q25.3   [Description]    (hg19-Feb_2009)
EnsemblCEP295NL - 17q25.3 [CytoView hg19]  CEP295NL - 17q25.3 [CytoView hg38]
Mapping of homologs : NCBICEP295NL [Mapview hg19]  CEP295NL [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK057217 DB037087
RefSeq transcript (Entrez)NM_001243540 NM_001243541
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)CEP295NL
Cluster EST : UnigeneHs.734636 [ NCBI ]
CGAP (NCI)Hs.734636
Alternative Splicing GalleryENSG00000178404
Gene ExpressionCEP295NL [ NCBI-GEO ]   CEP295NL [ EBI - ARRAY_EXPRESS ]   CEP295NL [ SEEK ]   CEP295NL [ MEM ]
Gene Expression Viewer (FireBrowse)CEP295NL [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100653515
GTEX Portal (Tissue expression)CEP295NL
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96MC4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96MC4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96MC4
Splice isoforms : SwissVarQ96MC4
PhosPhoSitePlusQ96MC4
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)CEP295NL
DMDM Disease mutations100653515
Blocks (Seattle)CEP295NL
SuperfamilyQ96MC4
Human Protein AtlasENSG00000178404
Peptide AtlasQ96MC4
Protein Interaction databases
DIP (DOE-UCLA)Q96MC4
IntAct (EBI)Q96MC4
FunCoupENSG00000178404
BioGRIDCEP295NL
STRING (EMBL)CEP295NL
ZODIACCEP295NL
Ontologies - Pathways
QuickGOQ96MC4
Ontology : AmiGOmotile cilium  
Ontology : EGO-EBImotile cilium  
NDEx NetworkCEP295NL
Atlas of Cancer Signalling NetworkCEP295NL
Wikipedia pathwaysCEP295NL
Orthology - Evolution
OrthoDB100653515
GeneTree (enSembl)ENSG00000178404
Phylogenetic Trees/Animal Genes : TreeFamCEP295NL
HOVERGENQ96MC4
HOGENOMQ96MC4
Homologs : HomoloGeneCEP295NL
Homology/Alignments : Family Browser (UCSC)CEP295NL
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerCEP295NL [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)CEP295NL
dbVarCEP295NL
ClinVarCEP295NL
1000_GenomesCEP295NL 
Exome Variant ServerCEP295NL
ExAC (Exome Aggregation Consortium)CEP295NL (select the gene name)
Genetic variants : HAPMAP100653515
Genomic Variants (DGV)CEP295NL [DGVbeta]
DECIPHERCEP295NL [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisCEP295NL 
Mutations
ICGC Data PortalCEP295NL 
TCGA Data PortalCEP295NL 
Broad Tumor PortalCEP295NL
OASIS PortalCEP295NL [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDCEP295NL
BioMutasearch CEP295NL
DgiDB (Drug Gene Interaction Database)CEP295NL
DoCM (Curated mutations)CEP295NL (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)CEP295NL (select a term)
intoGenCEP295NL
Cancer3DCEP295NL(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenCEP295NL
Genetic Testing Registry CEP295NL
NextProtQ96MC4 [Medical]
TSGene100653515
GENETestsCEP295NL
Target ValidationCEP295NL
Huge Navigator CEP295NL [HugePedia]
snp3D : Map Gene to Disease100653515
BioCentury BCIQCEP295NL
ClinGenCEP295NL
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100653515
Chemical/Pharm GKB GenePA166123697
Clinical trialCEP295NL
Miscellaneous
canSAR (ICR)CEP295NL (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineCEP295NL
EVEXCEP295NL
GoPubMedCEP295NL
iHOPCEP295NL
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 15:43:17 CEST 2017

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