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MAFIP (MAFF interacting protein (pseudogene))

Identity

Alias_namesMAFF interacting protein
Alias_symbol (synonym)FLJ35473
FLJ00219
FLJ39633
MIP
pp5644
TEKT4P4
Other alias
HGNC (Hugo) MAFIP
LocusID (NCBI) 727764
Atlas_Id 56010
Location -  [Link to chromosome band ]
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)MAFIP   31102
Cards
Entrez_Gene (NCBI)MAFIP  727764  MAFF interacting protein (pseudogene)
AliasesMIP; TEKT4P4; pp5644
GeneCards (Weizmann)MAFIP
Ensembl hg19 (Hinxton)ENSG00000277400 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000277400 [Gene_View]  - [Contig_View]  MAFIP [Vega]
ICGC DataPortalENSG00000277400
TCGA cBioPortalMAFIP
AceView (NCBI)MAFIP
Genatlas (Paris)MAFIP
WikiGenes727764
SOURCE (Princeton)MAFIP
Genetics Home Reference (NIH)MAFIP
Genomic and cartography
GoldenPath hg38 (UCSC)MAFIP  -  
GoldenPath hg19 (UCSC)MAFIP  -  
EnsemblMAFIP - [CytoView hg19]  MAFIP - [CytoView hg38]
Mapping of homologs : NCBIMAFIP [Mapview hg19]  MAFIP [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF289559 AK074146 AK096952 BG771232 CA419667
RefSeq transcript (Entrez)NM_001190825
RefSeq genomic (Entrez)NT_113888
Consensus coding sequences : CCDS (NCBI)MAFIP
Cluster EST : UnigeneHs.626311 [ NCBI ]
CGAP (NCI)Hs.626311
Alternative Splicing GalleryENSG00000277400
Gene ExpressionMAFIP [ NCBI-GEO ]   MAFIP [ EBI - ARRAY_EXPRESS ]   MAFIP [ SEEK ]   MAFIP [ MEM ]
Gene Expression Viewer (FireBrowse)MAFIP [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)727764
GTEX Portal (Tissue expression)MAFIP
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8WZ33   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8WZ33  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8WZ33
Splice isoforms : SwissVarQ8WZ33
PhosPhoSitePlusQ8WZ33
Domains : Interpro (EBI)Tektin   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MAFIP
DMDM Disease mutations727764
Blocks (Seattle)MAFIP
SuperfamilyQ8WZ33
Human Protein AtlasENSG00000277400
Peptide AtlasQ8WZ33
IPIIPI00737410   
Protein Interaction databases
DIP (DOE-UCLA)Q8WZ33
IntAct (EBI)Q8WZ33
FunCoupENSG00000277400
BioGRIDMAFIP
STRING (EMBL)MAFIP
ZODIACMAFIP
Ontologies - Pathways
QuickGOQ8WZ33
Ontology : AmiGOnucleus  nucleolus  cytoplasm  transcription, DNA-templated  regulation of transcription, DNA-templated  flagellated sperm motility  sperm flagellum  cilium assembly  cilium movement involved in cell motility  
Ontology : EGO-EBInucleus  nucleolus  cytoplasm  transcription, DNA-templated  regulation of transcription, DNA-templated  flagellated sperm motility  sperm flagellum  cilium assembly  cilium movement involved in cell motility  
NDEx NetworkMAFIP
Atlas of Cancer Signalling NetworkMAFIP
Wikipedia pathwaysMAFIP
Orthology - Evolution
OrthoDB727764
GeneTree (enSembl)ENSG00000277400
Phylogenetic Trees/Animal Genes : TreeFamMAFIP
HOVERGENQ8WZ33
HOGENOMQ8WZ33
Homologs : HomoloGeneMAFIP
Homology/Alignments : Family Browser (UCSC)MAFIP
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMAFIP [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MAFIP
dbVarMAFIP
ClinVarMAFIP
1000_GenomesMAFIP 
Exome Variant ServerMAFIP
ExAC (Exome Aggregation Consortium)MAFIP (select the gene name)
Genetic variants : HAPMAP727764
Genomic Variants (DGV)MAFIP [DGVbeta]
DECIPHERMAFIP [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMAFIP 
Mutations
ICGC Data PortalMAFIP 
TCGA Data PortalMAFIP 
Broad Tumor PortalMAFIP
OASIS PortalMAFIP [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDMAFIP
BioMutasearch MAFIP
DgiDB (Drug Gene Interaction Database)MAFIP
DoCM (Curated mutations)MAFIP (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MAFIP (select a term)
intoGenMAFIP
Cancer3DMAFIP(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMAFIP
Genetic Testing Registry MAFIP
NextProtQ8WZ33 [Medical]
TSGene727764
GENETestsMAFIP
Target ValidationMAFIP
Huge Navigator MAFIP [HugePedia]
snp3D : Map Gene to Disease727764
BioCentury BCIQMAFIP
ClinGenMAFIP
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD727764
Chemical/Pharm GKB GenePA164722169
Clinical trialMAFIP
Miscellaneous
canSAR (ICR)MAFIP (select the gene name)
Probes
Litterature
PubMed10 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMAFIP
EVEXMAFIP
GoPubMedMAFIP
iHOPMAFIP
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 25 19:16:51 CEST 2017

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