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MAIP1 (matrix AAA peptidase interacting protein 1)

Identity

Other aliasC2orf47
HGNC (Hugo) MAIP1
LocusID (NCBI) 79568
Atlas_Id 78741
Location 2q33.1  [Link to chromosome band 2q33]
Location_base_pair Starts at 199955317 and ends at 199964124 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)MAIP1   26198
Cards
Entrez_Gene (NCBI)MAIP1  79568  matrix AAA peptidase interacting protein 1
AliasesC2orf47
GeneCards (Weizmann)MAIP1
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr2:199955317-199964124 [Contig_View]  MAIP1 [Vega]
TCGA cBioPortalMAIP1
AceView (NCBI)MAIP1
Genatlas (Paris)MAIP1
WikiGenes79568
SOURCE (Princeton)MAIP1
Genetics Home Reference (NIH)MAIP1
Genomic and cartography
GoldenPath hg38 (UCSC)MAIP1  -     chr2:199955317-199964124 +  2q33.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MAIP1  -     2q33.1   [Description]    (hg19-Feb_2009)
EnsemblMAIP1 - 2q33.1 [CytoView hg19]  MAIP1 - 2q33.1 [CytoView hg38]
Mapping of homologs : NCBIMAIP1 [Mapview hg19]  MAIP1 [Mapview hg38]
OMIM617267   
Gene and transcription
Genbank (Entrez)AK026208 AL832964 BC017959 BQ448209 HQ447647
RefSeq transcript (Entrez)NM_024520
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MAIP1
Cluster EST : UnigeneHs.154494 [ NCBI ]
CGAP (NCI)Hs.154494
Gene ExpressionMAIP1 [ NCBI-GEO ]   MAIP1 [ EBI - ARRAY_EXPRESS ]   MAIP1 [ SEEK ]   MAIP1 [ MEM ]
Gene Expression Viewer (FireBrowse)MAIP1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)79568
GTEX Portal (Tissue expression)MAIP1
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8WWC4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8WWC4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8WWC4
Splice isoforms : SwissVarQ8WWC4
PhosPhoSitePlusQ8WWC4
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MAIP1
DMDM Disease mutations79568
Blocks (Seattle)MAIP1
SuperfamilyQ8WWC4
Peptide AtlasQ8WWC4
HPRD07994
IPIIPI00291751   IPI00927477   
Protein Interaction databases
DIP (DOE-UCLA)Q8WWC4
IntAct (EBI)Q8WWC4
BioGRIDMAIP1
STRING (EMBL)MAIP1
ZODIACMAIP1
Ontologies - Pathways
QuickGOQ8WWC4
Ontology : AmiGOprotein binding  mitochondrial inner membrane  mitochondrial matrix  inner mitochondrial membrane organization  protein insertion into mitochondrial membrane from inner side  mitochondrial calcium uptake  ribosome binding  protein insertion into mitochondrial membrane  mitochondrial calcium ion homeostasis  mitochondrial respiratory chain complex III biogenesis  mitochondrial respiratory chain complex IV biogenesis  
Ontology : EGO-EBIprotein binding  mitochondrial inner membrane  mitochondrial matrix  inner mitochondrial membrane organization  protein insertion into mitochondrial membrane from inner side  mitochondrial calcium uptake  ribosome binding  protein insertion into mitochondrial membrane  mitochondrial calcium ion homeostasis  mitochondrial respiratory chain complex III biogenesis  mitochondrial respiratory chain complex IV biogenesis  
NDEx NetworkMAIP1
Atlas of Cancer Signalling NetworkMAIP1
Wikipedia pathwaysMAIP1
Orthology - Evolution
OrthoDB79568
Phylogenetic Trees/Animal Genes : TreeFamMAIP1
HOVERGENQ8WWC4
HOGENOMQ8WWC4
Homologs : HomoloGeneMAIP1
Homology/Alignments : Family Browser (UCSC)MAIP1
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMAIP1 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MAIP1
dbVarMAIP1
ClinVarMAIP1
1000_GenomesMAIP1 
Exome Variant ServerMAIP1
ExAC (Exome Aggregation Consortium)MAIP1 (select the gene name)
Genetic variants : HAPMAP79568
Genomic Variants (DGV)MAIP1 [DGVbeta]
DECIPHERMAIP1 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMAIP1 
Mutations
ICGC Data PortalMAIP1 
TCGA Data PortalMAIP1 
Broad Tumor PortalMAIP1
OASIS PortalMAIP1 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDMAIP1
BioMutasearch MAIP1
DgiDB (Drug Gene Interaction Database)MAIP1
DoCM (Curated mutations)MAIP1 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MAIP1 (select a term)
intoGenMAIP1
Cancer3DMAIP1(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM617267   
Orphanet
MedgenMAIP1
Genetic Testing Registry MAIP1
NextProtQ8WWC4 [Medical]
TSGene79568
GENETestsMAIP1
Target ValidationMAIP1
Huge Navigator MAIP1 [HugePedia]
snp3D : Map Gene to Disease79568
BioCentury BCIQMAIP1
ClinGenMAIP1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD79568
Chemical/Pharm GKB GenePA162379149
Clinical trialMAIP1
Miscellaneous
canSAR (ICR)MAIP1 (select the gene name)
Probes
Litterature
PubMed16 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMAIP1
EVEXMAIP1
GoPubMedMAIP1
iHOPMAIP1
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 13:26:51 CEST 2017

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