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EAPP (E2F associated phosphoprotein)

Identity

Alias_namesC14orf11
chromosome 14 open reading frame 11
Alias_symbol (synonym)BM036
FLJ20578
Other alias
HGNC (Hugo) EAPP
LocusID (NCBI) 55837
Atlas_Id 56390
Location 14q13.1  [Link to chromosome band 14q13]
Location_base_pair Starts at 34985135 and ends at 35008943 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
EAPP (14q13.1) / SNX6 (14q13.1)EAPP (14q13.1) / USP13 (3q26.33)REST (4q12) / EAPP (14q13.1)

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)EAPP   19312
Cards
Entrez_Gene (NCBI)EAPP  55837  E2F associated phosphoprotein
AliasesBM036; C14orf11
GeneCards (Weizmann)EAPP
Ensembl hg19 (Hinxton)ENSG00000129518 [Gene_View]  chr14:34985135-35008943 [Contig_View]  EAPP [Vega]
Ensembl hg38 (Hinxton)ENSG00000129518 [Gene_View]  chr14:34985135-35008943 [Contig_View]  EAPP [Vega]
ICGC DataPortalENSG00000129518
TCGA cBioPortalEAPP
AceView (NCBI)EAPP
Genatlas (Paris)EAPP
WikiGenes55837
SOURCE (Princeton)EAPP
Genetics Home Reference (NIH)EAPP
Genomic and cartography
GoldenPath hg19 (UCSC)EAPP  -     chr14:34985135-35008943 -  14q13.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)EAPP  -     14q13.1   [Description]    (hg38-Dec_2013)
EnsemblEAPP - 14q13.1 [CytoView hg19]  EAPP - 14q13.1 [CytoView hg38]
Mapping of homologs : NCBIEAPP [Mapview hg19]  EAPP [Mapview hg38]
OMIM609486   
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)NM_001318916 NM_018453
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)EAPP
Cluster EST : UnigeneHs.433269 [ NCBI ]
CGAP (NCI)Hs.433269
Alternative Splicing GalleryENSG00000129518
Gene ExpressionEAPP [ NCBI-GEO ]   EAPP [ EBI - ARRAY_EXPRESS ]   EAPP [ SEEK ]   EAPP [ MEM ]
Gene Expression Viewer (FireBrowse)EAPP [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)55837
GTEX Portal (Tissue expression)EAPP
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ56P03   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ56P03  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ56P03
Splice isoforms : SwissVarQ56P03
PhosPhoSitePlusQ56P03
Domains : Interpro (EBI)E2F-assoc_phosphoprotein   
Domain families : Pfam (Sanger)Eapp_C (PF10238)   
Domain families : Pfam (NCBI)pfam10238   
Conserved Domain (NCBI)EAPP
DMDM Disease mutations55837
Blocks (Seattle)EAPP
SuperfamilyQ56P03
Human Protein AtlasENSG00000129518
Peptide AtlasQ56P03
HPRD12631
IPIIPI00306299   IPI01024895   IPI01024953   
Protein Interaction databases
DIP (DOE-UCLA)Q56P03
IntAct (EBI)Q56P03
FunCoupENSG00000129518
BioGRIDEAPP
STRING (EMBL)EAPP
ZODIACEAPP
Ontologies - Pathways
QuickGOQ56P03
Ontology : AmiGOnucleus  cytoplasm  Golgi apparatus  positive regulation of cell proliferation  positive regulation of transcription elongation from RNA polymerase II promoter  negative regulation of transcription elongation from RNA polymerase II promoter  
Ontology : EGO-EBInucleus  cytoplasm  Golgi apparatus  positive regulation of cell proliferation  positive regulation of transcription elongation from RNA polymerase II promoter  negative regulation of transcription elongation from RNA polymerase II promoter  
NDEx NetworkEAPP
Atlas of Cancer Signalling NetworkEAPP
Wikipedia pathwaysEAPP
Orthology - Evolution
OrthoDB55837
GeneTree (enSembl)ENSG00000129518
Phylogenetic Trees/Animal Genes : TreeFamEAPP
HOVERGENQ56P03
HOGENOMQ56P03
Homologs : HomoloGeneEAPP
Homology/Alignments : Family Browser (UCSC)EAPP
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerEAPP [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)EAPP
dbVarEAPP
ClinVarEAPP
1000_GenomesEAPP 
Exome Variant ServerEAPP
ExAC (Exome Aggregation Consortium)EAPP (select the gene name)
Genetic variants : HAPMAP55837
Genomic Variants (DGV)EAPP [DGVbeta]
DECIPHER (Syndromes)14:34985135-35008943  ENSG00000129518
CONAN: Copy Number AnalysisEAPP 
Mutations
ICGC Data PortalEAPP 
TCGA Data PortalEAPP 
Broad Tumor PortalEAPP
OASIS PortalEAPP [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICEAPP  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDEAPP
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 EAPP
DgiDB (Drug Gene Interaction Database)EAPP
DoCM (Curated mutations)EAPP (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)EAPP (select a term)
intoGenEAPP
Cancer3DEAPP(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM609486   
Orphanet
MedgenEAPP
Genetic Testing Registry EAPP
NextProtQ56P03 [Medical]
TSGene55837
GENETestsEAPP
Huge Navigator EAPP [HugePedia]
snp3D : Map Gene to Disease55837
BioCentury BCIQEAPP
ClinGenEAPP
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD55837
Chemical/Pharm GKB GenePA162384208
Clinical trialEAPP
Miscellaneous
canSAR (ICR)EAPP (select the gene name)
Probes
Litterature
PubMed20 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineEAPP
EVEXEAPP
GoPubMedEAPP
iHOPEAPP
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Thu Mar 30 14:59:37 CEST 2017

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