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MINAR2 (membrane integral NOTCH2 associated receptor 2)

Identity

Other aliasKIAA1024L
HGNC (Hugo) MINAR2
LocusID (NCBI) 100127206
Atlas_Id 80267
Location 5q23.3  [Link to chromosome band 5q23]
Location_base_pair Starts at 129748191 and ends at 129765063 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


External links

Nomenclature
HGNC (Hugo)MINAR2   33914
Cards
Entrez_Gene (NCBI)MINAR2  100127206  membrane integral NOTCH2 associated receptor 2
AliasesKIAA1024L
GeneCards (Weizmann)MINAR2
Ensembl hg19 (Hinxton)ENSG00000186367 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000186367 [Gene_View]  ENSG00000186367 [Sequence]  chr5:129748191-129765063 [Contig_View]  MINAR2 [Vega]
ICGC DataPortalENSG00000186367
TCGA cBioPortalMINAR2
AceView (NCBI)MINAR2
Genatlas (Paris)MINAR2
WikiGenes100127206
SOURCE (Princeton)MINAR2
Genetics Home Reference (NIH)MINAR2
Genomic and cartography
GoldenPath hg38 (UCSC)MINAR2  -     chr5:129748191-129765063 +  5q23.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MINAR2  -     5q23.3   [Description]    (hg19-Feb_2009)
GoldenPathMINAR2 - 5q23.3 [CytoView hg19]  MINAR2 - 5q23.3 [CytoView hg38]
ImmunoBaseENSG00000186367
Mapping of homologs : NCBIMINAR2 [Mapview hg19]  MINAR2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)DR731264
RefSeq transcript (Entrez)NM_001257308
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MINAR2
Cluster EST : UnigeneHs.582534 [ NCBI ]
CGAP (NCI)Hs.582534
Alternative Splicing GalleryENSG00000186367
Gene ExpressionMINAR2 [ NCBI-GEO ]   MINAR2 [ EBI - ARRAY_EXPRESS ]   MINAR2 [ SEEK ]   MINAR2 [ MEM ]
Gene Expression Viewer (FireBrowse)MINAR2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100127206
GTEX Portal (Tissue expression)MINAR2
Human Protein AtlasENSG00000186367-MINAR2 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtP59773   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP59773  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP59773
Splice isoforms : SwissVarP59773
PhosPhoSitePlusP59773
Domains : Interpro (EBI)UPF0258   
Domain families : Pfam (Sanger)UPF0258 (PF06789)   
Domain families : Pfam (NCBI)pfam06789   
Conserved Domain (NCBI)MINAR2
DMDM Disease mutations100127206
Blocks (Seattle)MINAR2
SuperfamilyP59773
Human Protein Atlas [tissue]ENSG00000186367-MINAR2 [tissue]
Peptide AtlasP59773
IPIIPI00402430   
Protein Interaction databases
DIP (DOE-UCLA)P59773
IntAct (EBI)P59773
FunCoupENSG00000186367
BioGRIDMINAR2
STRING (EMBL)MINAR2
ZODIACMINAR2
Ontologies - Pathways
QuickGOP59773
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkMINAR2
Atlas of Cancer Signalling NetworkMINAR2
Wikipedia pathwaysMINAR2
Orthology - Evolution
OrthoDB100127206
GeneTree (enSembl)ENSG00000186367
Phylogenetic Trees/Animal Genes : TreeFamMINAR2
HOGENOMP59773
Homologs : HomoloGeneMINAR2
Homology/Alignments : Family Browser (UCSC)MINAR2
Gene fusions - Rearrangements
Fusion : QuiverMINAR2
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMINAR2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MINAR2
dbVarMINAR2
ClinVarMINAR2
1000_GenomesMINAR2 
Exome Variant ServerMINAR2
ExAC (Exome Aggregation Consortium)ENSG00000186367
GNOMAD BrowserENSG00000186367
Varsome BrowserMINAR2
Genetic variants : HAPMAP100127206
Genomic Variants (DGV)MINAR2 [DGVbeta]
DECIPHERMINAR2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMINAR2 
Mutations
ICGC Data PortalMINAR2 
TCGA Data PortalMINAR2 
Broad Tumor PortalMINAR2
OASIS PortalMINAR2 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDMINAR2
BioMutasearch MINAR2
DgiDB (Drug Gene Interaction Database)MINAR2
DoCM (Curated mutations)MINAR2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MINAR2 (select a term)
intoGenMINAR2
Cancer3DMINAR2(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETMINAR2
MedgenMINAR2
Genetic Testing Registry MINAR2
NextProtP59773 [Medical]
TSGene100127206
GENETestsMINAR2
Target ValidationMINAR2
Huge Navigator MINAR2 [HugePedia]
snp3D : Map Gene to Disease100127206
BioCentury BCIQMINAR2
ClinGenMINAR2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100127206
Chemical/Pharm GKB GenePA162393049
Clinical trialMINAR2
Miscellaneous
canSAR (ICR)MINAR2 (select the gene name)
DataMed IndexMINAR2
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMINAR2
EVEXMINAR2
GoPubMedMINAR2
iHOPMINAR2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Sep 3 15:52:14 CEST 2019

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