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EID2 (EP300 interacting inhibitor of differentiation 2)

Identity

Alias_namesCRI2
CREBBP/EP300 inhibitory protein 2
CREBBP/EP300 inhibitor 2
Alias_symbol (synonym)EID-2
MGC20452
Other alias
HGNC (Hugo) EID2
LocusID (NCBI) 163126
Atlas_Id 50244
Location 19q13.2  [Link to chromosome band 19q13]
Location_base_pair Starts at 39538806 and ends at 39540198 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
EID2 (19q13.2) / EID2 (19q13.2)

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)EID2   28292
Cards
Entrez_Gene (NCBI)EID2  163126  EP300 interacting inhibitor of differentiation 2
AliasesCRI2; EID-2
GeneCards (Weizmann)EID2
Ensembl hg19 (Hinxton)ENSG00000176396 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000176396 [Gene_View]  chr19:39538806-39540198 [Contig_View]  EID2 [Vega]
ICGC DataPortalENSG00000176396
TCGA cBioPortalEID2
AceView (NCBI)EID2
Genatlas (Paris)EID2
WikiGenes163126
SOURCE (Princeton)EID2
Genetics Home Reference (NIH)EID2
Genomic and cartography
GoldenPath hg38 (UCSC)EID2  -     chr19:39538806-39540198 -  19q13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)EID2  -     19q13.2   [Description]    (hg19-Feb_2009)
EnsemblEID2 - 19q13.2 [CytoView hg19]  EID2 - 19q13.2 [CytoView hg38]
Mapping of homologs : NCBIEID2 [Mapview hg19]  EID2 [Mapview hg38]
OMIM609773   
Gene and transcription
Genbank (Entrez)AK128468 AY251272 BC030137 BC099899
RefSeq transcript (Entrez)NM_153232
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)EID2
Cluster EST : UnigeneHs.18949 [ NCBI ]
CGAP (NCI)Hs.18949
Alternative Splicing GalleryENSG00000176396
Gene ExpressionEID2 [ NCBI-GEO ]   EID2 [ EBI - ARRAY_EXPRESS ]   EID2 [ SEEK ]   EID2 [ MEM ]
Gene Expression Viewer (FireBrowse)EID2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)163126
GTEX Portal (Tissue expression)EID2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N6I1   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N6I1  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N6I1
Splice isoforms : SwissVarQ8N6I1
PhosPhoSitePlusQ8N6I1
Domains : Interpro (EBI)EID    EID-2   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)EID2
DMDM Disease mutations163126
Blocks (Seattle)EID2
SuperfamilyQ8N6I1
Human Protein AtlasENSG00000176396
Peptide AtlasQ8N6I1
HPRD16754
IPIIPI00879045   IPI00879914   IPI00167014   
Protein Interaction databases
DIP (DOE-UCLA)Q8N6I1
IntAct (EBI)Q8N6I1
FunCoupENSG00000176396
BioGRIDEID2
STRING (EMBL)EID2
ZODIACEID2
Ontologies - Pathways
QuickGOQ8N6I1
Ontology : AmiGOnegative regulation of transcription from RNA polymerase II promoter  protein binding  intracellular  nucleoplasm  transcription, DNA-templated  transforming growth factor beta receptor complex assembly  SMAD protein complex assembly  muscle organ development  regulation of transforming growth factor beta receptor signaling pathway  cell differentiation  negative regulation of transforming growth factor beta receptor signaling pathway  regulation of cell proliferation  negative regulation of transcription, DNA-templated  SMAD binding  
Ontology : EGO-EBInegative regulation of transcription from RNA polymerase II promoter  protein binding  intracellular  nucleoplasm  transcription, DNA-templated  transforming growth factor beta receptor complex assembly  SMAD protein complex assembly  muscle organ development  regulation of transforming growth factor beta receptor signaling pathway  cell differentiation  negative regulation of transforming growth factor beta receptor signaling pathway  regulation of cell proliferation  negative regulation of transcription, DNA-templated  SMAD binding  
NDEx NetworkEID2
Atlas of Cancer Signalling NetworkEID2
Wikipedia pathwaysEID2
Orthology - Evolution
OrthoDB163126
GeneTree (enSembl)ENSG00000176396
Phylogenetic Trees/Animal Genes : TreeFamEID2
HOVERGENQ8N6I1
HOGENOMQ8N6I1
Homologs : HomoloGeneEID2
Homology/Alignments : Family Browser (UCSC)EID2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerEID2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)EID2
dbVarEID2
ClinVarEID2
1000_GenomesEID2 
Exome Variant ServerEID2
ExAC (Exome Aggregation Consortium)EID2 (select the gene name)
Genetic variants : HAPMAP163126
Genomic Variants (DGV)EID2 [DGVbeta]
DECIPHEREID2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisEID2 
Mutations
ICGC Data PortalEID2 
TCGA Data PortalEID2 
Broad Tumor PortalEID2
OASIS PortalEID2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICEID2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDEID2
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 EID2
DgiDB (Drug Gene Interaction Database)EID2
DoCM (Curated mutations)EID2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)EID2 (select a term)
intoGenEID2
Cancer3DEID2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM609773   
Orphanet
MedgenEID2
Genetic Testing Registry EID2
NextProtQ8N6I1 [Medical]
TSGene163126
GENETestsEID2
Target ValidationEID2
Huge Navigator EID2 [HugePedia]
snp3D : Map Gene to Disease163126
BioCentury BCIQEID2
ClinGenEID2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD163126
Chemical/Pharm GKB GenePA162384544
Clinical trialEID2
Miscellaneous
canSAR (ICR)EID2 (select the gene name)
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineEID2
EVEXEID2
GoPubMedEID2
iHOPEID2
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 12:32:17 CEST 2017

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