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ENHO (energy homeostasis associated)

Identity

Alias_namesC9orf165
chromosome 9 open reading frame 165
Alias_symbol (synonym)UNQ470
Other alias
HGNC (Hugo) ENHO
LocusID (NCBI) 375704
Atlas_Id 55931
Location 9p13.3  [Link to chromosome band 9p13]
Location_base_pair Starts at 34521042 and ends at 34523039 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)
UNC13B (9p13.3) / ENHO (9p13.3)

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)ENHO   24838
Cards
Entrez_Gene (NCBI)ENHO  375704  energy homeostasis associated
AliasesC9orf165; UNQ470
GeneCards (Weizmann)ENHO
Ensembl hg19 (Hinxton)ENSG00000168913 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000168913 [Gene_View]  chr9:34521042-34523039 [Contig_View]  ENHO [Vega]
ICGC DataPortalENSG00000168913
TCGA cBioPortalENHO
AceView (NCBI)ENHO
Genatlas (Paris)ENHO
WikiGenes375704
SOURCE (Princeton)ENHO
Genetics Home Reference (NIH)ENHO
Genomic and cartography
GoldenPath hg38 (UCSC)ENHO  -     chr9:34521042-34523039 -  9p13.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ENHO  -     9p13.3   [Description]    (hg19-Feb_2009)
EnsemblENHO - 9p13.3 [CytoView hg19]  ENHO - 9p13.3 [CytoView hg38]
Mapping of homologs : NCBIENHO [Mapview hg19]  ENHO [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI554721 AY358658 BC022101 BQ932712 BX111579
RefSeq transcript (Entrez)NM_198573
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ENHO
Cluster EST : UnigeneHs.522085 [ NCBI ]
CGAP (NCI)Hs.522085
Alternative Splicing GalleryENSG00000168913
Gene ExpressionENHO [ NCBI-GEO ]   ENHO [ EBI - ARRAY_EXPRESS ]   ENHO [ SEEK ]   ENHO [ MEM ]
Gene Expression Viewer (FireBrowse)ENHO [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)375704
GTEX Portal (Tissue expression)ENHO
Human Protein AtlasENSG00000168913-ENHO [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6UWT2   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6UWT2  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6UWT2
Splice isoforms : SwissVarQ6UWT2
PhosPhoSitePlusQ6UWT2
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)ENHO
DMDM Disease mutations375704
Blocks (Seattle)ENHO
SuperfamilyQ6UWT2
Human Protein Atlas [tissue]ENSG00000168913-ENHO [tissue]
Peptide AtlasQ6UWT2
HPRD18263
IPIIPI00847642   IPI00166942   
Protein Interaction databases
DIP (DOE-UCLA)Q6UWT2
IntAct (EBI)Q6UWT2
FunCoupENSG00000168913
BioGRIDENHO
STRING (EMBL)ENHO
ZODIACENHO
Ontologies - Pathways
QuickGOQ6UWT2
Ontology : AmiGOextracellular region  plasma membrane  positive regulation of Notch signaling pathway  
Ontology : EGO-EBIextracellular region  plasma membrane  positive regulation of Notch signaling pathway  
NDEx NetworkENHO
Atlas of Cancer Signalling NetworkENHO
Wikipedia pathwaysENHO
Orthology - Evolution
OrthoDB375704
GeneTree (enSembl)ENSG00000168913
Phylogenetic Trees/Animal Genes : TreeFamENHO
HOVERGENQ6UWT2
HOGENOMQ6UWT2
Homologs : HomoloGeneENHO
Homology/Alignments : Family Browser (UCSC)ENHO
Gene fusions - Rearrangements
Tumor Fusion PortalENHO
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerENHO [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ENHO
dbVarENHO
ClinVarENHO
1000_GenomesENHO 
Exome Variant ServerENHO
ExAC (Exome Aggregation Consortium)ENSG00000168913
GNOMAD BrowserENSG00000168913
Genetic variants : HAPMAP375704
Genomic Variants (DGV)ENHO [DGVbeta]
DECIPHERENHO [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisENHO 
Mutations
ICGC Data PortalENHO 
TCGA Data PortalENHO 
Broad Tumor PortalENHO
OASIS PortalENHO [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICENHO  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDENHO
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ENHO
DgiDB (Drug Gene Interaction Database)ENHO
DoCM (Curated mutations)ENHO (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ENHO (select a term)
intoGenENHO
Cancer3DENHO(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETENHO
MedgenENHO
Genetic Testing Registry ENHO
NextProtQ6UWT2 [Medical]
TSGene375704
GENETestsENHO
Target ValidationENHO
Huge Navigator ENHO [HugePedia]
snp3D : Map Gene to Disease375704
BioCentury BCIQENHO
ClinGenENHO
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD375704
Chemical/Pharm GKB GenePA164719156
Clinical trialENHO
Miscellaneous
canSAR (ICR)ENHO (select the gene name)
Probes
Litterature
PubMed25 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineENHO
EVEXENHO
GoPubMedENHO
iHOPENHO
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Nov 21 14:12:02 CET 2017

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