Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

MAFIP (MAFF interacting protein (pseudogene))

Identity

Alias (NCBI)MIP
TEKT4P4
pp5644
HGNC (Hugo) MAFIP
HGNC Alias symbFLJ35473
FLJ00219
FLJ39633
MIP
pp5644
TEKT4P4
HGNC Alias nametektin 4 pseudogene 4
HGNC Previous nameMAFF interacting protein
LocusID (NCBI) 727764
Atlas_Id 56010
Location -  [Link to chromosome band ]
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)MAFIP   31102
Cards
Entrez_Gene (NCBI)MAFIP    MAFF interacting protein (pseudogene)
AliasesMIP; TEKT4P4; pp5644
GeneCards (Weizmann)MAFIP
Ensembl hg19 (Hinxton)ENSG00000277400 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000277400 [Gene_View]  ENSG00000277400 [Sequence]  - [Contig_View]  MAFIP [Vega]
ICGC DataPortalENSG00000277400
TCGA cBioPortalMAFIP
AceView (NCBI)MAFIP
Genatlas (Paris)MAFIP
SOURCE (Princeton)MAFIP
Genetics Home Reference (NIH)MAFIP
Genomic and cartography
GoldenPath hg38 (UCSC)MAFIP  -  
GoldenPath hg19 (UCSC)MAFIP  -  
GoldenPathMAFIP - [CytoView hg19]  MAFIP - [CytoView hg38]
ImmunoBaseENSG00000277400
Genome Data Viewer NCBIMAFIP [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AF289559 AK074146 AK096952 BG771232 CA419667
RefSeq transcript (Entrez)NM_001190825
Consensus coding sequences : CCDS (NCBI)MAFIP
Gene ExpressionMAFIP [ NCBI-GEO ]   MAFIP [ EBI - ARRAY_EXPRESS ]   MAFIP [ SEEK ]   MAFIP [ MEM ]
Gene Expression Viewer (FireBrowse)MAFIP [ Firebrowse - Broad ]
GenevisibleExpression of MAFIP in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)727764
GTEX Portal (Tissue expression)MAFIP
Human Protein AtlasENSG00000277400-MAFIP [pathology]   [cell]   [tissue]
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
PhosPhoSitePlusQ8WZ33
Domains : Interpro (EBI)Tektin   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MAFIP
SuperfamilyQ8WZ33
AlphaFold pdb e-kbQ8WZ33   
Human Protein Atlas [tissue]ENSG00000277400-MAFIP [tissue]
Protein Interaction databases
DIP (DOE-UCLA)Q8WZ33
IntAct (EBI)Q8WZ33
BioGRIDMAFIP
STRING (EMBL)MAFIP
ZODIACMAFIP
Ontologies - Pathways
QuickGOQ8WZ33
Ontology : AmiGOnucleolus  cytoplasm  microtubule cytoskeleton  sperm flagellum  cilium assembly  cilium movement involved in cell motility  
Ontology : EGO-EBInucleolus  cytoplasm  microtubule cytoskeleton  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
Homologs : HomoloGeneMAFIP
Homology/Alignments : Family Browser (UCSC)MAFIP
Gene fusions - Rearrangements
Fusion : QuiverMAFIP
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMAFIP [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MAFIP
dbVarMAFIP
ClinVarMAFIP
MonarchMAFIP
1000_GenomesMAFIP 
Exome Variant ServerMAFIP
GNOMAD BrowserENSG00000277400
Varsome BrowserMAFIP
ACMGMAFIP variants
VarityQ8WZ33
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
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaMAFIP
DgiDB (Drug Gene Interaction Database)MAFIP
DoCM (Curated mutations)MAFIP
CIViC (Clinical Interpretations of Variants in Cancer)MAFIP
Cancer3DMAFIP
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETMAFIP
MedgenMAFIP
Genetic Testing Registry MAFIP
NextProtQ8WZ33 [Medical]
GENETestsMAFIP
Target ValidationMAFIP
Huge Navigator MAFIP [HugePedia]
ClinGenMAFIP
Clinical trials, drugs, therapy
MyCancerGenomeMAFIP
Protein Interactions : CTDMAFIP
Pharm GKB GenePA164722169
PharosQ8WZ33
Clinical trialMAFIP
Miscellaneous
canSAR (ICR)MAFIP
HarmonizomeMAFIP
DataMed IndexMAFIP
Probes
Litterature
PubMed11 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXMAFIP
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Oct 4 15:17:26 CEST 2021

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.