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MICU3 (mitochondrial calcium uptake family member 3)

Identity

Alias_namesEFHA2
EF hand domain family A2
EF-hand domain family, member A2
mitochondrial calcium uptake family, member 3
Alias_symbol (synonym)DKFZp313A0139
Other alias
HGNC (Hugo) MICU3
LocusID (NCBI) 286097
Atlas_Id 68979
Location 8p22  [Link to chromosome band 8p22]
Location_base_pair Starts at 17027238 and ends at 17122639 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
ZNF804A (2q32.1) / MICU3 (8p22)

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)MICU3   27820 Cards Entrez_Gene (NCBI)MICU3  286097  mitochondrial calcium uptake family member 3 AliasesEFHA2 GeneCards (Weizmann)MICU3 Ensembl hg19 (Hinxton)ENSG00000155970 [Gene_View] Ensembl hg38 (Hinxton)ENSG00000155970 [Gene_View]  chr8:17027238-17122639 [Contig_View]  MICU3 [Vega] ICGC DataPortalENSG00000155970 TCGA cBioPortalMICU3 AceView (NCBI)MICU3 Genatlas (Paris)MICU3 WikiGenes286097 SOURCE (Princeton)MICU3 Genetics Home Reference (NIH)MICU3 Genomic and cartography GoldenPath hg38 (UCSC)MICU3  -     chr8:17027238-17122639 +  8p22   [Description]    (hg38-Dec_2013) GoldenPath hg19 (UCSC)MICU3  -     8p22   [Description]    (hg19-Feb_2009) EnsemblMICU3 - 8p22 [CytoView hg19]  MICU3 - 8p22 [CytoView hg38] Mapping of homologs : NCBIMICU3 [Mapview hg19]  MICU3 [Mapview hg38] OMIM610633    Gene and transcription Genbank (Entrez)AL833419 BC032868 BC045553 BI546243 BX953026 RefSeq transcript (Entrez)NM_001349810 NM_181723 RefSeq genomic (Entrez) Consensus coding sequences : CCDS (NCBI)MICU3 Cluster EST : UnigeneHs.403594 [ NCBI ] CGAP (NCI)Hs.403594 Alternative Splicing GalleryENSG00000155970 Gene ExpressionMICU3 [ NCBI-GEO ]   MICU3 [ EBI - ARRAY_EXPRESS ]   MICU3 [ SEEK ]   MICU3 [ MEM ] Gene Expression Viewer (FireBrowse)MICU3 [ Firebrowse - Broad ] SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60] GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]   BioGPS (Tissue expression)286097 GTEX Portal (Tissue expression)MICU3 Protein : pattern, domain, 3D structure UniProt/SwissProtQ86XE3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction] NextProtQ86XE3  [Sequence]  [Exons]  [Medical]  [Publications] With graphics : InterProQ86XE3 Splice isoforms : SwissVarQ86XE3 PhosPhoSitePlusQ86XE3 Domaine pattern : Prosite (Expaxy)EF_HAND_1 (PS00018)    EF_HAND_2 (PS50222)    Domains : Interpro (EBI)EF-hand-dom_pair    EF_Hand_1_Ca_BS    EF_hand_dom    Domain families : Pfam (Sanger)EF-hand_8 (PF13833)    Domain families : Pfam (NCBI)pfam13833    Domain families : Smart (EMBL)EFh (SM00054)   Conserved Domain (NCBI)MICU3 DMDM Disease mutations286097 Blocks (Seattle)MICU3 SuperfamilyQ86XE3 Human Protein AtlasENSG00000155970 Peptide AtlasQ86XE3 HPRD13264 IPIIPI00329209   IPI00983867   IPI00982794    Protein Interaction databases DIP (DOE-UCLA)Q86XE3 IntAct (EBI)Q86XE3 FunCoupENSG00000155970 BioGRIDMICU3 STRING (EMBL)MICU3 ZODIACMICU3 Ontologies - Pathways QuickGOQ86XE3 Ontology : AmiGOcalcium ion binding  mitochondrion  integral component of membrane   Ontology : EGO-EBIcalcium ion binding  mitochondrion  integral component of membrane   NDEx NetworkMICU3 Atlas of Cancer Signalling NetworkMICU3 Wikipedia pathwaysMICU3 Orthology - Evolution OrthoDB286097 GeneTree (enSembl)ENSG00000155970 Phylogenetic Trees/Animal Genes : TreeFamMICU3 HOVERGENQ86XE3 HOGENOMQ86XE3 Homologs : HomoloGeneMICU3 Homology/Alignments : Family Browser (UCSC)MICU3 Gene fusions - Rearrangements Polymorphisms : SNP and Copy number variants NCBI Variation ViewerMICU3 [hg38] dbSNP Single Nucleotide Polymorphism (NCBI)MICU3 dbVarMICU3 ClinVarMICU3 1000_GenomesMICU3  Exome Variant ServerMICU3 ExAC (Exome Aggregation Consortium)MICU3 (select the gene name) Genetic variants : HAPMAP286097 Genomic Variants (DGV)MICU3 [DGVbeta] DECIPHERMICU3 [patients]   [syndromes]   [variants]   [genes]   CONAN: Copy Number AnalysisMICU3  Mutations ICGC Data PortalMICU3  TCGA Data PortalMICU3  Broad Tumor PortalMICU3 OASIS PortalMICU3 [ Somatic mutations - Copy number] Mutations and Diseases : HGMDMICU3 BioMutasearch MICU3 DgiDB (Drug Gene Interaction Database)MICU3 DoCM (Curated mutations)MICU3 (select the gene name) CIViC (Clinical Interpretations of Variants in Cancer)MICU3 (select a term) intoGenMICU3 Cancer3DMICU3(select the gene name) Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser] DiseasesOMIM610633    Orphanet MedgenMICU3 Genetic Testing Registry MICU3 NextProtQ86XE3 [Medical] TSGene286097 GENETestsMICU3 Target ValidationMICU3 Huge Navigator MICU3 [HugePedia] snp3D : Map Gene to Disease286097 BioCentury BCIQMICU3 ClinGenMICU3 Clinical trials, drugs, therapyChemical/Protein Interactions : CTD286097 Chemical/Pharm GKB GenePA134953154 Clinical trialMICU3 MiscellaneouscanSAR (ICR)MICU3 (select the gene name) ProbesLitteraturePubMed5 Pubmed reference(s) in Entrez GeneRIFsGene References Into Functions (Entrez) CoreMineMICU3 EVEXMICU3 GoPubMedMICU3 iHOPMICU3

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