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DAP (death-associated protein)

Identity

HGNC (Hugo) DAP
LocusID (NCBI) 1611
Atlas_Id 40261
Location 5p15.2
Location_base_pair Starts at 10679342 and ends at 10761387 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2015)
DAP 5p15.2 / RGL2 6p21.32DAP 5p15.2 / SNX9 6q25.3LPCAT1 5p15.33 / DAP 5p15.2
SNX9 6q25.3 / DAP 5p15.2

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)DAP   2672
Cards
Entrez_Gene (NCBI)DAP  1611  death-associated protein
GeneCards (Weizmann)DAP
Ensembl hg19 (Hinxton)ENSG00000112977 [Gene_View]  chr5:10679342-10761387 [Contig_View]  DAP [Vega]
Ensembl hg38 (Hinxton)ENSG00000112977 [Gene_View]  chr5:10679342-10761387 [Contig_View]  DAP [Vega]
ICGC DataPortalENSG00000112977
TCGA cBioPortalDAP
AceView (NCBI)DAP
Genatlas (Paris)DAP
WikiGenes1611
SOURCE (Princeton)DAP
Genomic and cartography
GoldenPath hg19 (UCSC)DAP  -     chr5:10679342-10761387 -  5p15.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)DAP  -     5p15.2   [Description]    (hg38-Dec_2013)
EnsemblDAP - 5p15.2 [CytoView hg19]  DAP - 5p15.2 [CytoView hg38]
Mapping of homologs : NCBIDAP [Mapview hg19]  DAP [Mapview hg38]
OMIM600954   
Gene and transcription
Genbank (Entrez)AK298670 AK311783 BC002726 BI823002 BP265421
RefSeq transcript (Entrez)NM_001291963 NM_004394
RefSeq genomic (Entrez)NC_000005 NC_018916 NG_011546 NT_006576 NW_004929321
Consensus coding sequences : CCDS (NCBI)DAP
Cluster EST : UnigeneHs.75189 [ NCBI ]
CGAP (NCI)Hs.75189
Alternative Splicing : Fast-db (Paris)GSHG0024655
Alternative Splicing GalleryENSG00000112977
Gene ExpressionDAP [ NCBI-GEO ]     DAP [ SEEK ]   DAP [ MEM ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)1611
Protein : pattern, domain, 3D structure
UniProt/SwissProtP51397 (Uniprot)
NextProtP51397  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP51397
Splice isoforms : SwissVarP51397 (Swissvar)
PhosPhoSitePlusP51397
Domains : Interpro (EBI)DAP1/DAPL1   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
DMDM Disease mutations1611
Blocks (Seattle)DAP
Human Protein AtlasENSG00000112977
Peptide AtlasP51397
HPRD02977
IPIIPI00018117   IPI00030844   IPI00911094   
Protein Interaction databases
DIP (DOE-UCLA)P51397
IntAct (EBI)P51397
FunCoupENSG00000112977
BioGRIDDAP
IntegromeDBDAP
STRING (EMBL)DAP
ZODIACDAP
Ontologies - Pathways
QuickGOP51397
Ontology : AmiGOautophagy  apoptotic process  activation of cysteine-type endopeptidase activity involved in apoptotic process  negative regulation of autophagy  negative regulation of NF-kappaB transcription factor activity  cellular response to amino acid starvation  negative regulation of transcription, DNA-templated  death domain binding  apoptotic signaling pathway  
Ontology : EGO-EBIautophagy  apoptotic process  activation of cysteine-type endopeptidase activity involved in apoptotic process  negative regulation of autophagy  negative regulation of NF-kappaB transcription factor activity  cellular response to amino acid starvation  negative regulation of transcription, DNA-templated  death domain binding  apoptotic signaling pathway  
Protein Interaction DatabaseDAP
Atlas of Cancer Signalling NetworkDAP
Wikipedia pathwaysDAP
Orthology - Evolution
OrthoDB1611
GeneTree (enSembl)ENSG00000112977
Phylogenetic Trees/Animal Genes : TreeFamDAP
Homologs : HomoloGeneDAP
Homology/Alignments : Family Browser (UCSC)DAP
Gene fusions - Rearrangements
Fusion: TCGADAP 5p15.2 RGL2 6p21.32 PRAD
Fusion: TCGADAP 5p15.2 SNX9 6q25.3 BRCA
Fusion: TCGALPCAT1 5p15.33 DAP 5p15.2 KIRC
Fusion: TCGASNX9 6q25.3 DAP 5p15.2 BRCA
Polymorphisms : SNP, variants
NCBI Variation ViewerDAP [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)DAP
dbVarDAP
ClinVarDAP
1000_GenomesDAP 
Exome Variant ServerDAP
Exome Aggregation Consortium (ExAC)ENSG00000112977
SNP (GeneSNP Utah)DAP
SNP : HGBaseDAP
Genetic variants : HAPMAPDAP
Genomic Variants (DGV)DAP [DGVbeta]
Mutations
ICGC Data PortalDAP 
TCGA Data PortalDAP 
Tumor PortalDAP
TCGA Copy Number PortalDAP
Somatic Mutations in Cancer : COSMICDAP 
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 DAP
DgiDB (Drug Gene Interaction Database)DAP
DoCM (Curated mutations)DAP (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)DAP (select a term)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] 
Diseases
DECIPHER (Syndromes)5:10679342-10761387
CONAN: Copy Number AnalysisDAP 
Mutations and Diseases : HGMDDAP
OMIM600954   
MedgenDAP
NextProtP51397 [Medical]
TSGene1611
GENETestsDAP
Huge Navigator DAP [HugePedia]  DAP [HugeCancerGEM]
snp3D : Map Gene to Disease1611
BioCentury BCIQDAP
General knowledge
Chemical/Protein Interactions : CTD1611
Chemical/Pharm GKB GenePA27140
Clinical trialDAP
Other databases
Probes
Litterature
PubMed20 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineDAP
GoPubMedDAP
iHOPDAP
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Sat Jan 16 18:26:52 CET 2016

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