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MBLAC2 (metallo-beta-lactamase domain containing 2)

Identity

Alias_symbol (synonym)DKFZp686P15118
MGC46734
Other alias-
HGNC (Hugo) MBLAC2
LocusID (NCBI) 153364
Atlas_Id 68831
Location 5q14.3  [Link to chromosome band 5q14]
Location_base_pair Starts at 90458203 and ends at 90474768 bp from pter ( according to hg38-Dec_2013)

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)MBLAC2   33711
Cards
Entrez_Gene (NCBI)MBLAC2  153364  metallo-beta-lactamase domain containing 2
Aliases
GeneCards (Weizmann)MBLAC2
Ensembl hg19 (Hinxton)ENSG00000176055 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000176055 [Gene_View]  chr5:90458203-90474768 [Contig_View]  MBLAC2 [Vega]
ICGC DataPortalENSG00000176055
TCGA cBioPortalMBLAC2
AceView (NCBI)MBLAC2
Genatlas (Paris)MBLAC2
WikiGenes153364
SOURCE (Princeton)MBLAC2
Genetics Home Reference (NIH)MBLAC2
Genomic and cartography
GoldenPath hg38 (UCSC)MBLAC2  -     chr5:90458203-90474768 -  5q14.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MBLAC2  -     5q14.3   [Description]    (hg19-Feb_2009)
EnsemblMBLAC2 - 5q14.3 [CytoView hg19]  MBLAC2 - 5q14.3 [CytoView hg38]
Mapping of homologs : NCBIMBLAC2 [Mapview hg19]  MBLAC2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI288430 AK096942 AK128603 AK289778 BC038230
RefSeq transcript (Entrez)NM_203406
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MBLAC2
Cluster EST : UnigeneHs.64004 [ NCBI ]
CGAP (NCI)Hs.64004
Alternative Splicing GalleryENSG00000176055
Gene ExpressionMBLAC2 [ NCBI-GEO ]   MBLAC2 [ EBI - ARRAY_EXPRESS ]   MBLAC2 [ SEEK ]   MBLAC2 [ MEM ]
Gene Expression Viewer (FireBrowse)MBLAC2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)153364
GTEX Portal (Tissue expression)MBLAC2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ68D91   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ68D91  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ68D91
Splice isoforms : SwissVarQ68D91
PhosPhoSitePlusQ68D91
Domains : Interpro (EBI)Metallo-B-lactamas   
Domain families : Pfam (Sanger)Lactamase_B (PF00753)   
Domain families : Pfam (NCBI)pfam00753   
Domain families : Smart (EMBL)Lactamase_B (SM00849)  
Conserved Domain (NCBI)MBLAC2
DMDM Disease mutations153364
Blocks (Seattle)MBLAC2
SuperfamilyQ68D91
Human Protein AtlasENSG00000176055
Peptide AtlasQ68D91
HPRD14099
IPIIPI00293336   IPI00888973   IPI01013975   
Protein Interaction databases
DIP (DOE-UCLA)Q68D91
IntAct (EBI)Q68D91
FunCoupENSG00000176055
BioGRIDMBLAC2
STRING (EMBL)MBLAC2
ZODIACMBLAC2
Ontologies - Pathways
QuickGOQ68D91
Ontology : AmiGOmolecular_function  biological_process  hydrolase activity  metal ion binding  extracellular exosome  
Ontology : EGO-EBImolecular_function  biological_process  hydrolase activity  metal ion binding  extracellular exosome  
NDEx NetworkMBLAC2
Atlas of Cancer Signalling NetworkMBLAC2
Wikipedia pathwaysMBLAC2
Orthology - Evolution
OrthoDB153364
GeneTree (enSembl)ENSG00000176055
Phylogenetic Trees/Animal Genes : TreeFamMBLAC2
HOVERGENQ68D91
HOGENOMQ68D91
Homologs : HomoloGeneMBLAC2
Homology/Alignments : Family Browser (UCSC)MBLAC2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMBLAC2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MBLAC2
dbVarMBLAC2
ClinVarMBLAC2
1000_GenomesMBLAC2 
Exome Variant ServerMBLAC2
ExAC (Exome Aggregation Consortium)MBLAC2 (select the gene name)
Genetic variants : HAPMAP153364
Genomic Variants (DGV)MBLAC2 [DGVbeta]
DECIPHERMBLAC2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMBLAC2 
Mutations
ICGC Data PortalMBLAC2 
TCGA Data PortalMBLAC2 
Broad Tumor PortalMBLAC2
OASIS PortalMBLAC2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMBLAC2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMBLAC2
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 MBLAC2
DgiDB (Drug Gene Interaction Database)MBLAC2
DoCM (Curated mutations)MBLAC2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MBLAC2 (select a term)
intoGenMBLAC2
Cancer3DMBLAC2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMBLAC2
Genetic Testing Registry MBLAC2
NextProtQ68D91 [Medical]
TSGene153364
GENETestsMBLAC2
Target ValidationMBLAC2
Huge Navigator MBLAC2 [HugePedia]
snp3D : Map Gene to Disease153364
BioCentury BCIQMBLAC2
ClinGenMBLAC2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD153364
Chemical/Pharm GKB GenePA164722236
Clinical trialMBLAC2
Miscellaneous
canSAR (ICR)MBLAC2 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMBLAC2
EVEXMBLAC2
GoPubMedMBLAC2
iHOPMBLAC2
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 13:27:00 CEST 2017

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