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ENGASE (endo-beta-N-acetylglucosaminidase)

Identity

Alias_symbol (synonym)FLJ21865
Other alias-
HGNC (Hugo) ENGASE
LocusID (NCBI) 64772
Atlas_Id 62830
Location 17q25.3  [Link to chromosome band 17q25]
Location_base_pair Starts at 79074937 and ends at 79088603 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
AES (19p13.3) / ENGASE (17q25.3)ENGASE (17q25.3) / COL5A2 (2q32.2)ENGASE (17q25.3) / ENGASE (17q25.3)

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)ENGASE   24622
Cards
Entrez_Gene (NCBI)ENGASE  64772  endo-beta-N-acetylglucosaminidase
Aliases
GeneCards (Weizmann)ENGASE
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr17:79074937-79088603 [Contig_View]  ENGASE [Vega]
TCGA cBioPortalENGASE
AceView (NCBI)ENGASE
Genatlas (Paris)ENGASE
WikiGenes64772
SOURCE (Princeton)ENGASE
Genetics Home Reference (NIH)ENGASE
Genomic and cartography
GoldenPath hg38 (UCSC)ENGASE  -     chr17:79074937-79088603 +  17q25.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ENGASE  -     17q25.3   [Description]    (hg19-Feb_2009)
EnsemblENGASE - 17q25.3 [CytoView hg19]  ENGASE - 17q25.3 [CytoView hg38]
Mapping of homologs : NCBIENGASE [Mapview hg19]  ENGASE [Mapview hg38]
OMIM611898   
Gene and transcription
Genbank (Entrez)AF512564 AK025518 AK301115 AL110283 BC024213
RefSeq transcript (Entrez)NM_001042573 NM_022759
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ENGASE
Cluster EST : UnigeneHs.29288 [ NCBI ]
CGAP (NCI)Hs.29288
Gene ExpressionENGASE [ NCBI-GEO ]   ENGASE [ EBI - ARRAY_EXPRESS ]   ENGASE [ SEEK ]   ENGASE [ MEM ]
Gene Expression Viewer (FireBrowse)ENGASE [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)64772
GTEX Portal (Tissue expression)ENGASE
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8NFI3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8NFI3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8NFI3
Splice isoforms : SwissVarQ8NFI3
PhosPhoSitePlusQ8NFI3
Domaine pattern : Prosite (Expaxy)BRCT (PS50172)   
Domains : Interpro (EBI)BRCT_dom    ENGase    Glyco_hydro_85   
Domain families : Pfam (Sanger)Glyco_hydro_85 (PF03644)   
Domain families : Pfam (NCBI)pfam03644   
Conserved Domain (NCBI)ENGASE
DMDM Disease mutations64772
Blocks (Seattle)ENGASE
SuperfamilyQ8NFI3
Peptide AtlasQ8NFI3
HPRD10978
IPIIPI00168838   IPI00874016   IPI00889689   IPI01018828   
Protein Interaction databases
DIP (DOE-UCLA)Q8NFI3
IntAct (EBI)Q8NFI3
BioGRIDENGASE
STRING (EMBL)ENGASE
ZODIACENGASE
Ontologies - Pathways
QuickGOQ8NFI3
Ontology : AmiGOlysosome  cytosol  protein folding  protein deglycosylation  mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase activity  
Ontology : EGO-EBIlysosome  cytosol  protein folding  protein deglycosylation  mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase activity  
Pathways : KEGGOther glycan degradation   
NDEx NetworkENGASE
Atlas of Cancer Signalling NetworkENGASE
Wikipedia pathwaysENGASE
Orthology - Evolution
OrthoDB64772
Phylogenetic Trees/Animal Genes : TreeFamENGASE
HOVERGENQ8NFI3
HOGENOMQ8NFI3
Homologs : HomoloGeneENGASE
Homology/Alignments : Family Browser (UCSC)ENGASE
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerENGASE [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ENGASE
dbVarENGASE
ClinVarENGASE
1000_GenomesENGASE 
Exome Variant ServerENGASE
ExAC (Exome Aggregation Consortium)ENGASE (select the gene name)
Genetic variants : HAPMAP64772
Genomic Variants (DGV)ENGASE [DGVbeta]
DECIPHERENGASE [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisENGASE 
Mutations
ICGC Data PortalENGASE 
TCGA Data PortalENGASE 
Broad Tumor PortalENGASE
OASIS PortalENGASE [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICENGASE  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDENGASE
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 ENGASE
DgiDB (Drug Gene Interaction Database)ENGASE
DoCM (Curated mutations)ENGASE (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ENGASE (select a term)
intoGenENGASE
Cancer3DENGASE(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM611898   
Orphanet
MedgenENGASE
Genetic Testing Registry ENGASE
NextProtQ8NFI3 [Medical]
TSGene64772
GENETestsENGASE
Target ValidationENGASE
Huge Navigator ENGASE [HugePedia]
snp3D : Map Gene to Disease64772
BioCentury BCIQENGASE
ClinGenENGASE
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD64772
Chemical/Pharm GKB GenePA164719123
Clinical trialENGASE
Miscellaneous
canSAR (ICR)ENGASE (select the gene name)
Probes
Litterature
PubMed10 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineENGASE
EVEXENGASE
GoPubMedENGASE
iHOPENGASE
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:07:06 CEST 2017

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