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MBIP (MAP3K12 binding inhibitory protein 1)

Identity

Alias (NCBI)-
HGNC (Hugo) MBIP
LocusID (NCBI) 51562
Atlas_Id 54445
Location 14q13.3  [Link to chromosome band 14q13]
Location_base_pair Starts at 36298564 and ends at 36320637 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
AXL (19q13.2) / MBIP (14q13.3)MBIP (14q13.3) / LINC01599 (14q21.3)MBIP (14q13.3) / PCLO (7q21.11)

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)MBIP   20427
Cards
Entrez_Gene (NCBI)MBIP    MAP3K12 binding inhibitory protein 1
Aliases
GeneCards (Weizmann)MBIP
Ensembl hg19 (Hinxton)ENSG00000151332 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000151332 [Gene_View]  ENSG00000151332 [Sequence]  chr14:36298564-36320637 [Contig_View]  MBIP [Vega]
ICGC DataPortalENSG00000151332
TCGA cBioPortalMBIP
AceView (NCBI)MBIP
Genatlas (Paris)MBIP
SOURCE (Princeton)MBIP
Genetics Home Reference (NIH)MBIP
Genomic and cartography
GoldenPath hg38 (UCSC)MBIP  -     chr14:36298564-36320637 -  14q13.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MBIP  -     14q13.3   [Description]    (hg19-Feb_2009)
GoldenPathMBIP - 14q13.3 [CytoView hg19]  MBIP - 14q13.3 [CytoView hg38]
ImmunoBaseENSG00000151332
Genome Data Viewer NCBIMBIP [Mapview hg19]  
OMIM609431   
Gene and transcription
Genbank (Entrez)AA761503 AB038523 AF208857 AK293473 AK315290
RefSeq transcript (Entrez)NM_001144891 NM_001308110 NM_016586
Consensus coding sequences : CCDS (NCBI)MBIP
Gene ExpressionMBIP [ NCBI-GEO ]   MBIP [ EBI - ARRAY_EXPRESS ]   MBIP [ SEEK ]   MBIP [ MEM ]
Gene Expression Viewer (FireBrowse)MBIP [ Firebrowse - Broad ]
GenevisibleExpression of MBIP in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)51562
GTEX Portal (Tissue expression)MBIP
Human Protein AtlasENSG00000151332-MBIP [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9NS73   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9NS73  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9NS73
PhosPhoSitePlusQ9NS73
Domains : Interpro (EBI)MBIP   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MBIP
SuperfamilyQ9NS73
AlphaFold pdb e-kbQ9NS73   
Human Protein Atlas [tissue]ENSG00000151332-MBIP [tissue]
HPRD14368
Protein Interaction databases
DIP (DOE-UCLA)Q9NS73
IntAct (EBI)Q9NS73
BioGRIDMBIP
STRING (EMBL)MBIP
ZODIACMBIP
Ontologies - Pathways
QuickGOQ9NS73
Ontology : AmiGOprotein kinase inhibitor activity  protein binding  nucleoplasm  Ada2/Gcn5/Ada3 transcription activator complex  nucleolus  cytosol  cytosol  negative regulation of protein kinase activity  positive regulation of gene expression  identical protein binding  histone H3 acetylation  positive regulation of JNK cascade  
Ontology : EGO-EBIprotein kinase inhibitor activity  protein binding  nucleoplasm  Ada2/Gcn5/Ada3 transcription activator complex  nucleolus  cytosol  cytosol  negative regulation of protein kinase activity  positive regulation of gene expression  identical protein binding  histone H3 acetylation  positive regulation of JNK cascade  
NDEx NetworkMBIP
Atlas of Cancer Signalling NetworkMBIP
Wikipedia pathwaysMBIP
Orthology - Evolution
OrthoDB51562
GeneTree (enSembl)ENSG00000151332
Phylogenetic Trees/Animal Genes : TreeFamMBIP
Homologs : HomoloGeneMBIP
Homology/Alignments : Family Browser (UCSC)MBIP
Gene fusions - Rearrangements
Fusion : MitelmanAXL/MBIP [19q13.2/14q13.3]  
Fusion : MitelmanMBIP/C14orf183 [14q13.3/t(14;14)(q13;q21)]  
Fusion Cancer (Beijing)AXL [19q13.2]  -  MBIP [14q13.3]  [FUSC003133]
Fusion : QuiverMBIP
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMBIP [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MBIP
dbVarMBIP
ClinVarMBIP
MonarchMBIP
1000_GenomesMBIP 
Exome Variant ServerMBIP
GNOMAD BrowserENSG00000151332
Varsome BrowserMBIP
ACMGMBIP variants
VarityQ9NS73
Genomic Variants (DGV)MBIP [DGVbeta]
DECIPHERMBIP [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMBIP 
Mutations
ICGC Data PortalMBIP 
TCGA Data PortalMBIP 
Broad Tumor PortalMBIP
OASIS PortalMBIP [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMBIP  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DMBIP
Mutations and Diseases : HGMDMBIP
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaMBIP
DgiDB (Drug Gene Interaction Database)MBIP
DoCM (Curated mutations)MBIP
CIViC (Clinical Interpretations of Variants in Cancer)MBIP
Cancer3DMBIP
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM609431   
Orphanet
DisGeNETMBIP
MedgenMBIP
Genetic Testing Registry MBIP
NextProtQ9NS73 [Medical]
GENETestsMBIP
Target ValidationMBIP
Huge Navigator MBIP [HugePedia]
ClinGenMBIP
Clinical trials, drugs, therapy
MyCancerGenomeMBIP
Protein Interactions : CTDMBIP
Pharm GKB GenePA134929415
PharosQ9NS73
Clinical trialMBIP
Miscellaneous
canSAR (ICR)MBIP
HarmonizomeMBIP
DataMed IndexMBIP
Probes
Litterature
PubMed41 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXMBIP
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:17:59 CEST 2021

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