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MIIP (migration and invasion inhibitory protein)

Identity

Alias_symbol (synonym)FLJ12438
IIp45
Other aliasIIP45
HGNC (Hugo) MIIP
LocusID (NCBI) 60672
Atlas_Id 50899
Location 1p36.22  [Link to chromosome band 1p36]
Location_base_pair Starts at 12019242 and ends at 12032049 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
MIIP (1p36.22) / CMYA5 (5q14.1)MIIP 1p36.22 / CMYA5 5q14.1

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)MIIP   25715
Cards
Entrez_Gene (NCBI)MIIP  60672  migration and invasion inhibitory protein
AliasesIIP45
GeneCards (Weizmann)MIIP
Ensembl hg19 (Hinxton)ENSG00000116691 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000116691 [Gene_View]  chr1:12019242-12032049 [Contig_View]  MIIP [Vega]
ICGC DataPortalENSG00000116691
TCGA cBioPortalMIIP
AceView (NCBI)MIIP
Genatlas (Paris)MIIP
WikiGenes60672
SOURCE (Princeton)MIIP
Genetics Home Reference (NIH)MIIP
Genomic and cartography
GoldenPath hg38 (UCSC)MIIP  -     chr1:12019242-12032049 +  1p36.22   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIIP  -     1p36.22   [Description]    (hg19-Feb_2009)
EnsemblMIIP - 1p36.22 [CytoView hg19]  MIIP - 1p36.22 [CytoView hg38]
Mapping of homologs : NCBIMIIP [Mapview hg19]  MIIP [Mapview hg38]
OMIM608772   
Gene and transcription
Genbank (Entrez)AK022500 AK024020 AK095928 AW196459 BC008068
RefSeq transcript (Entrez)NM_001025374 NM_021933
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIIP
Cluster EST : UnigeneHs.8595 [ NCBI ]
CGAP (NCI)Hs.8595
Alternative Splicing GalleryENSG00000116691
Gene ExpressionMIIP [ NCBI-GEO ]   MIIP [ EBI - ARRAY_EXPRESS ]   MIIP [ SEEK ]   MIIP [ MEM ]
Gene Expression Viewer (FireBrowse)MIIP [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)60672
GTEX Portal (Tissue expression)MIIP
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5JXC2   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5JXC2  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5JXC2
Splice isoforms : SwissVarQ5JXC2
PhosPhoSitePlusQ5JXC2
Domains : Interpro (EBI)MIIP   
Domain families : Pfam (Sanger)MIIP (PF15734)   
Domain families : Pfam (NCBI)pfam15734   
Conserved Domain (NCBI)MIIP
DMDM Disease mutations60672
Blocks (Seattle)MIIP
SuperfamilyQ5JXC2
Human Protein AtlasENSG00000116691
Peptide AtlasQ5JXC2
HPRD07768
IPIIPI00551070   IPI00887912   IPI00952982   
Protein Interaction databases
DIP (DOE-UCLA)Q5JXC2
IntAct (EBI)Q5JXC2
FunCoupENSG00000116691
BioGRIDMIIP
STRING (EMBL)MIIP
ZODIACMIIP
Ontologies - Pathways
QuickGOQ5JXC2
Ontology : AmiGOprotein binding  negative regulation of G2/M transition of mitotic cell cycle  negative regulation of cell migration  
Ontology : EGO-EBIprotein binding  negative regulation of G2/M transition of mitotic cell cycle  negative regulation of cell migration  
NDEx NetworkMIIP
Atlas of Cancer Signalling NetworkMIIP
Wikipedia pathwaysMIIP
Orthology - Evolution
OrthoDB60672
GeneTree (enSembl)ENSG00000116691
Phylogenetic Trees/Animal Genes : TreeFamMIIP
HOVERGENQ5JXC2
HOGENOMQ5JXC2
Homologs : HomoloGeneMIIP
Homology/Alignments : Family Browser (UCSC)MIIP
Gene fusions - Rearrangements
Fusion : MitelmanMIIP/CMYA5 [1p36.22/5q14.1]  
Fusion: TCGAMIIP 1p36.22 CMYA5 5q14.1 GBM
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMIIP [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MIIP
dbVarMIIP
ClinVarMIIP
1000_GenomesMIIP 
Exome Variant ServerMIIP
ExAC (Exome Aggregation Consortium)MIIP (select the gene name)
Genetic variants : HAPMAP60672
Genomic Variants (DGV)MIIP [DGVbeta]
DECIPHERMIIP [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMIIP 
Mutations
ICGC Data PortalMIIP 
TCGA Data PortalMIIP 
Broad Tumor PortalMIIP
OASIS PortalMIIP [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMIIP  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMIIP
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 MIIP
DgiDB (Drug Gene Interaction Database)MIIP
DoCM (Curated mutations)MIIP (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MIIP (select a term)
intoGenMIIP
Cancer3DMIIP(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM608772   
Orphanet
MedgenMIIP
Genetic Testing Registry MIIP
NextProtQ5JXC2 [Medical]
TSGene60672
GENETestsMIIP
Huge Navigator MIIP [HugePedia]
snp3D : Map Gene to Disease60672
BioCentury BCIQMIIP
ClinGenMIIP
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD60672
Chemical/Pharm GKB GenePA165751598
Clinical trialMIIP
Miscellaneous
canSAR (ICR)MIIP (select the gene name)
Probes
Litterature
PubMed16 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIIP
EVEXMIIP
GoPubMedMIIP
iHOPMIIP
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Fri May 19 12:24:58 CEST 2017

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