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MIER2 (MIER family member 2)

Identity

Alias_namesKIAA1193
KIAA1193
mesoderm induction early response 1, family member 2
Other aliasMi-er2
HGNC (Hugo) MIER2
LocusID (NCBI) 54531
Atlas_Id 54459
Location 19p13.3  [Link to chromosome band 19p13]
Location_base_pair Starts at 305575 and ends at 344791 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
MIER2 (19p13.3) / CDK5RAP1 (20q11.21)MIER2 (19p13.3) / NMRK2 (19p13.3)MIER2 (19p13.3) / RSRC2 (12q24.31)
MIER2 19p13.3 / CDK5RAP1 20q11.21

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

 


Other Solid tumors implicated (Data extracted from papers in the Atlas) [ 1 ]
  Lung: Translocations in Adenocarcinoma


External links

Nomenclature
HGNC (Hugo)MIER2   29210
Cards
Entrez_Gene (NCBI)MIER2  54531  MIER family member 2
AliasesKIAA1193; Mi-er2
GeneCards (Weizmann)MIER2
Ensembl hg19 (Hinxton)ENSG00000105556 [Gene_View]  chr19:305575-344791 [Contig_View]  MIER2 [Vega]
Ensembl hg38 (Hinxton)ENSG00000105556 [Gene_View]  chr19:305575-344791 [Contig_View]  MIER2 [Vega]
ICGC DataPortalENSG00000105556
TCGA cBioPortalMIER2
AceView (NCBI)MIER2
Genatlas (Paris)MIER2
WikiGenes54531
SOURCE (Princeton)MIER2
Genetics Home Reference (NIH)MIER2
Genomic and cartography
GoldenPath hg19 (UCSC)MIER2  -     chr19:305575-344791 -  19p13.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIER2  -     19p13.3   [Description]    (hg38-Dec_2013)
EnsemblMIER2 - 19p13.3 [CytoView hg19]  MIER2 - 19p13.3 [CytoView hg38]
Mapping of homologs : NCBIMIER2 [Mapview hg19]  MIER2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB033019 BC028203
RefSeq transcript (Entrez)NM_017550
RefSeq genomic (Entrez)NC_000019 NC_018930 NT_011295 NW_004929412
Consensus coding sequences : CCDS (NCBI)MIER2
Cluster EST : UnigeneHs.101891 [ NCBI ]
CGAP (NCI)Hs.101891
Alternative Splicing GalleryENSG00000105556
Gene ExpressionMIER2 [ NCBI-GEO ]   MIER2 [ EBI - ARRAY_EXPRESS ]   MIER2 [ SEEK ]   MIER2 [ MEM ]
Gene Expression Viewer (FireBrowse)MIER2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)54531
GTEX Portal (Tissue expression)MIER2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N344   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N344  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N344
Splice isoforms : SwissVarQ8N344
PhosPhoSitePlusQ8N344
Domaine pattern : Prosite (Expaxy)ELM2 (PS51156)    SANT (PS51293)   
Domains : Interpro (EBI)ELM2_dom    Homeodomain-like    SANT/Myb    SANT_dom   
Domain families : Pfam (Sanger)ELM2 (PF01448)   
Domain families : Pfam (NCBI)pfam01448   
Domain families : Smart (EMBL)SANT (SM00717)  
Conserved Domain (NCBI)MIER2
DMDM Disease mutations54531
Blocks (Seattle)MIER2
SuperfamilyQ8N344
Human Protein AtlasENSG00000105556
Peptide AtlasQ8N344
HPRD11130
IPIIPI00297301   
Protein Interaction databases
DIP (DOE-UCLA)Q8N344
IntAct (EBI)Q8N344
FunCoupENSG00000105556
BioGRIDMIER2
STRING (EMBL)MIER2
ZODIACMIER2
Ontologies - Pathways
QuickGOQ8N344
Ontology : AmiGODNA binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  
Ontology : EGO-EBIDNA binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  
NDEx NetworkMIER2
Atlas of Cancer Signalling NetworkMIER2
Wikipedia pathwaysMIER2
Orthology - Evolution
OrthoDB54531
GeneTree (enSembl)ENSG00000105556
Phylogenetic Trees/Animal Genes : TreeFamMIER2
HOVERGENQ8N344
HOGENOMQ8N344
Homologs : HomoloGeneMIER2
Homology/Alignments : Family Browser (UCSC)MIER2
Gene fusions - Rearrangements
Fusion : MitelmanMIER2/CDK5RAP1 [19p13.3/20q11.21]  
Fusion : MitelmanMIER2/NMRK2 [19p13.3/19p13.3]  [t(19;19)(p13;p13)]  
Fusion : MitelmanMIER2/RSRC2 [19p13.3/12q24.31]  [t(12;19)(q24;p13)]  
Fusion: TCGAMIER2 19p13.3 CDK5RAP1 20q11.21 BLCA
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMIER2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MIER2
dbVarMIER2
ClinVarMIER2
1000_GenomesMIER2 
Exome Variant ServerMIER2
ExAC (Exome Aggregation Consortium)MIER2 (select the gene name)
Genetic variants : HAPMAP54531
Genomic Variants (DGV)MIER2 [DGVbeta]
DECIPHER (Syndromes)19:305575-344791  ENSG00000105556
CONAN: Copy Number AnalysisMIER2 
Mutations
ICGC Data PortalMIER2 
TCGA Data PortalMIER2 
Broad Tumor PortalMIER2
OASIS PortalMIER2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMIER2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMIER2
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 MIER2
DgiDB (Drug Gene Interaction Database)MIER2
DoCM (Curated mutations)MIER2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MIER2 (select a term)
intoGenMIER2
Cancer3DMIER2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMIER2
Genetic Testing Registry MIER2
NextProtQ8N344 [Medical]
TSGene54531
GENETestsMIER2
Huge Navigator MIER2 [HugePedia]
snp3D : Map Gene to Disease54531
BioCentury BCIQMIER2
ClinGenMIER2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD54531
Chemical/Pharm GKB GenePA134925804
Clinical trialMIER2
Miscellaneous
canSAR (ICR)MIER2 (select the gene name)
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIER2
EVEXMIER2
GoPubMedMIER2
iHOPMIER2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Thu Mar 30 15:09:11 CEST 2017

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