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MAP10 (microtubule associated protein 10)

Identity

Alias_namesKIAA1383
KIAA1383
Alias_symbol (synonym)MTR120
Other alias
HGNC (Hugo) MAP10
LocusID (NCBI) 54627
Atlas_Id 68789
Location 1q42.2  [Link to chromosome band 1q42]
Location_base_pair Starts at 232804892 and ends at 232810346 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)MAP10   29265
Cards
Entrez_Gene (NCBI)MAP10  54627  microtubule associated protein 10
AliasesKIAA1383; MTR120
GeneCards (Weizmann)MAP10
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr1:232804892-232810346 [Contig_View]  MAP10 [Vega]
TCGA cBioPortalMAP10
AceView (NCBI)MAP10
Genatlas (Paris)MAP10
WikiGenes54627
SOURCE (Princeton)MAP10
Genetics Home Reference (NIH)MAP10
Genomic and cartography
GoldenPath hg38 (UCSC)MAP10  -     chr1:232804892-232810346 +  1q42.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MAP10  -     1q42.2   [Description]    (hg19-Feb_2009)
EnsemblMAP10 - 1q42.2 [CytoView hg19]  MAP10 - 1q42.2 [CytoView hg38]
Mapping of homologs : NCBIMAP10 [Mapview hg19]  MAP10 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB037804 AK290216 BC036663 BC109122
RefSeq transcript (Entrez)NM_019090
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MAP10
Cluster EST : UnigeneHs.160373 [ NCBI ]
CGAP (NCI)Hs.160373
Gene ExpressionMAP10 [ NCBI-GEO ]   MAP10 [ EBI - ARRAY_EXPRESS ]   MAP10 [ SEEK ]   MAP10 [ MEM ]
Gene Expression Viewer (FireBrowse)MAP10 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)54627
GTEX Portal (Tissue expression)MAP10
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9P2G4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9P2G4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9P2G4
Splice isoforms : SwissVarQ9P2G4
PhosPhoSitePlusQ9P2G4
Domains : Interpro (EBI)MAP10   
Domain families : Pfam (Sanger)HPHLAWLY (PF14925)   
Domain families : Pfam (NCBI)pfam14925   
Conserved Domain (NCBI)MAP10
DMDM Disease mutations54627
Blocks (Seattle)MAP10
SuperfamilyQ9P2G4
Peptide AtlasQ9P2G4
IPIIPI00847373   
Protein Interaction databases
DIP (DOE-UCLA)Q9P2G4
IntAct (EBI)Q9P2G4
BioGRIDMAP10
STRING (EMBL)MAP10
ZODIACMAP10
Ontologies - Pathways
QuickGOQ9P2G4
Ontology : AmiGOcentrosome  cytoplasmic microtubule  microtubule binding  midbody  cytoplasmic microtubule organization  positive regulation of cytokinesis  regulation of microtubule-based process  mitotic spindle midzone assembly  cell division  mitotic spindle pole  mitotic spindle midzone  
Ontology : EGO-EBIcentrosome  cytoplasmic microtubule  microtubule binding  midbody  cytoplasmic microtubule organization  positive regulation of cytokinesis  regulation of microtubule-based process  mitotic spindle midzone assembly  cell division  mitotic spindle pole  mitotic spindle midzone  
NDEx NetworkMAP10
Atlas of Cancer Signalling NetworkMAP10
Wikipedia pathwaysMAP10
Orthology - Evolution
OrthoDB54627
Phylogenetic Trees/Animal Genes : TreeFamMAP10
HOVERGENQ9P2G4
HOGENOMQ9P2G4
Homologs : HomoloGeneMAP10
Homology/Alignments : Family Browser (UCSC)MAP10
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMAP10 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MAP10
dbVarMAP10
ClinVarMAP10
1000_GenomesMAP10 
Exome Variant ServerMAP10
ExAC (Exome Aggregation Consortium)MAP10 (select the gene name)
Genetic variants : HAPMAP54627
Genomic Variants (DGV)MAP10 [DGVbeta]
DECIPHERMAP10 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMAP10 
Mutations
ICGC Data PortalMAP10 
TCGA Data PortalMAP10 
Broad Tumor PortalMAP10
OASIS PortalMAP10 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDMAP10
BioMutasearch MAP10
DgiDB (Drug Gene Interaction Database)MAP10
DoCM (Curated mutations)MAP10 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MAP10 (select a term)
intoGenMAP10
Cancer3DMAP10(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMAP10
Genetic Testing Registry MAP10
NextProtQ9P2G4 [Medical]
TSGene54627
GENETestsMAP10
Target ValidationMAP10
Huge Navigator MAP10 [HugePedia]
snp3D : Map Gene to Disease54627
BioCentury BCIQMAP10
ClinGenMAP10
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD54627
Chemical/Pharm GKB GenePA142671610
Clinical trialMAP10
Miscellaneous
canSAR (ICR)MAP10 (select the gene name)
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMAP10
EVEXMAP10
GoPubMedMAP10
iHOPMAP10
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed May 31 15:25:28 CEST 2017

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