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EZHIP (EZH inhibitory protein)

Identity

Alias_namesCXorf67
chromosome X open reading frame 67
Alias_symbol (synonym)CATACOMB
Other aliasKIP75
HGNC (Hugo) EZHIP
LocusID (NCBI) 340602
Atlas_Id 53814
Location Xp11.22  [Link to chromosome band Xp11]
Location_base_pair Starts at 51406915 and ends at 51408837 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)
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


Other Solid tumors implicated (Data extracted from papers in the Atlas) [ 1 ]

Solid Tumors EndometrStromSarctX17ID6633


External links

Nomenclature
HGNC (Hugo)EZHIP   33738
Cards
Entrez_Gene (NCBI)EZHIP  340602  EZH inhibitory protein
AliasesCATACOMB; CXorf67; KIP75
GeneCards (Weizmann)EZHIP
Ensembl hg19 (Hinxton)ENSG00000187690 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000187690 [Gene_View]  ENSG00000187690 [Sequence]  chrX:51406915-51408837 [Contig_View]  EZHIP [Vega]
ICGC DataPortalENSG00000187690
TCGA cBioPortalEZHIP
AceView (NCBI)EZHIP
Genatlas (Paris)EZHIP
WikiGenes340602
SOURCE (Princeton)EZHIP
Genetics Home Reference (NIH)EZHIP
Genomic and cartography
GoldenPath hg38 (UCSC)EZHIP  -     chrX:51406915-51408837 +  -   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)EZHIP  -     -   [Description]    (hg19-Feb_2009)
GoldenPathEZHIP - - [CytoView hg19]  EZHIP - - [CytoView hg38]
ImmunoBaseENSG00000187690
Mapping of homologs : NCBIEZHIP [Mapview hg19]  EZHIP [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC046248 MK321327
RefSeq transcript (Entrez)NM_203407
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)EZHIP
Cluster EST : UnigeneHs.97053 [ NCBI ]
CGAP (NCI)Hs.97053
Alternative Splicing GalleryENSG00000187690
Gene ExpressionEZHIP [ NCBI-GEO ]   EZHIP [ EBI - ARRAY_EXPRESS ]   EZHIP [ SEEK ]   EZHIP [ MEM ]
Gene Expression Viewer (FireBrowse)EZHIP [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)340602
GTEX Portal (Tissue expression)EZHIP
Human Protein AtlasENSG00000187690-EZHIP [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ86X51   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ86X51  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ86X51
Splice isoforms : SwissVarQ86X51
PhosPhoSitePlusQ86X51
Domains : Interpro (EBI)PBMUCL2   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)EZHIP
DMDM Disease mutations340602
Blocks (Seattle)EZHIP
SuperfamilyQ86X51
Human Protein Atlas [tissue]ENSG00000187690-EZHIP [tissue]
Peptide AtlasQ86X51
HPRD14176
IPIIPI00257965   
Protein Interaction databases
DIP (DOE-UCLA)Q86X51
IntAct (EBI)Q86X51
FunCoupENSG00000187690
BioGRIDEZHIP
STRING (EMBL)EZHIP
ZODIACEZHIP
Ontologies - Pathways
QuickGOQ86X51
Ontology : AmiGOprotein binding  nucleus  nucleoplasm  cytosol  negative regulation of histone H3-K27 methylation  
Ontology : EGO-EBIprotein binding  nucleus  nucleoplasm  cytosol  negative regulation of histone H3-K27 methylation  
NDEx NetworkEZHIP
Atlas of Cancer Signalling NetworkEZHIP
Wikipedia pathwaysEZHIP
Orthology - Evolution
OrthoDB340602
GeneTree (enSembl)ENSG00000187690
Phylogenetic Trees/Animal Genes : TreeFamEZHIP
HOGENOMQ86X51
Homologs : HomoloGeneEZHIP
Homology/Alignments : Family Browser (UCSC)EZHIP
Gene fusions - Rearrangements
Fusion : MitelmanMBTD1/CXorf67 [17q21.33/Xp11.22]  [t(X;17)(p11;q21)]  
Fusion : QuiverEZHIP
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerEZHIP [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)EZHIP
dbVarEZHIP
ClinVarEZHIP
1000_GenomesEZHIP 
Exome Variant ServerEZHIP
ExAC (Exome Aggregation Consortium)ENSG00000187690
GNOMAD BrowserENSG00000187690
Varsome BrowserEZHIP
Genetic variants : HAPMAP340602
Genomic Variants (DGV)EZHIP [DGVbeta]
DECIPHEREZHIP [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisEZHIP 
Mutations
ICGC Data PortalEZHIP 
TCGA Data PortalEZHIP 
Broad Tumor PortalEZHIP
OASIS PortalEZHIP [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDEZHIP
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch EZHIP
DgiDB (Drug Gene Interaction Database)EZHIP
DoCM (Curated mutations)EZHIP (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)EZHIP (select a term)
intoGenEZHIP
Cancer3DEZHIP(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETEZHIP
MedgenEZHIP
Genetic Testing Registry EZHIP
NextProtQ86X51 [Medical]
TSGene340602
GENETestsEZHIP
Target ValidationEZHIP
Huge Navigator EZHIP [HugePedia]
snp3D : Map Gene to Disease340602
BioCentury BCIQEZHIP
ClinGenEZHIP
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD340602
Chemical/Pharm GKB GenePA166049013
Clinical trialEZHIP
Miscellaneous
canSAR (ICR)EZHIP (select the gene name)
DataMed IndexEZHIP
Probes
Litterature
PubMed11 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineEZHIP
EVEXEZHIP
GoPubMedEZHIP
iHOPEZHIP
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Aug 26 18:07:47 CEST 2019

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