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M1AP (meiosis 1 associated protein)

Identity

Alias_namesC2orf65
chromosome 2 open reading frame 65
Alias_symbol (synonym)D6Mm5e
SPATA37
Other alias
HGNC (Hugo) M1AP
LocusID (NCBI) 130951
Atlas_Id 68744
Location 2p13.1  [Link to chromosome band 2p13]
Location_base_pair Starts at 74802387 and ends at 74875465 bp from pter ( according to hg19-Feb_2009)

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)M1AP   25183
Cards
Entrez_Gene (NCBI)M1AP  130951  meiosis 1 associated protein
AliasesC2orf65; D6Mm5e; SPATA37
GeneCards (Weizmann)M1AP
Ensembl hg19 (Hinxton)ENSG00000159374 [Gene_View]  chr2:74802387-74875465 [Contig_View]  M1AP [Vega]
Ensembl hg38 (Hinxton)ENSG00000159374 [Gene_View]  chr2:74802387-74875465 [Contig_View]  M1AP [Vega]
ICGC DataPortalENSG00000159374
TCGA cBioPortalM1AP
AceView (NCBI)M1AP
Genatlas (Paris)M1AP
WikiGenes130951
SOURCE (Princeton)M1AP
Genetics Home Reference (NIH)M1AP
Genomic and cartography
GoldenPath hg19 (UCSC)M1AP  -     chr2:74802387-74875465 -  2p13.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)M1AP  -     2p13.1   [Description]    (hg38-Dec_2013)
EnsemblM1AP - 2p13.1 [CytoView hg19]  M1AP - 2p13.1 [CytoView hg38]
Mapping of homologs : NCBIM1AP [Mapview hg19]  M1AP [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK126374 AK130161 AK300188 BC014602 BC025997
RefSeq transcript (Entrez)NM_001281295 NM_001281296 NM_138804
RefSeq genomic (Entrez)NC_000002 NC_018913 NT_022184 NW_004929300
Consensus coding sequences : CCDS (NCBI)M1AP
Cluster EST : UnigeneHs.348645 [ NCBI ]
CGAP (NCI)Hs.348645
Alternative Splicing GalleryENSG00000159374
Gene ExpressionM1AP [ NCBI-GEO ]   M1AP [ EBI - ARRAY_EXPRESS ]   M1AP [ SEEK ]   M1AP [ MEM ]
Gene Expression Viewer (FireBrowse)M1AP [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)130951
GTEX Portal (Tissue expression)M1AP
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8TC57   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8TC57  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8TC57
Splice isoforms : SwissVarQ8TC57
PhosPhoSitePlusQ8TC57
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)M1AP
DMDM Disease mutations130951
Blocks (Seattle)M1AP
SuperfamilyQ8TC57
Human Protein AtlasENSG00000159374
Peptide AtlasQ8TC57
HPRD14047
IPIIPI00290903   IPI00442818   IPI00902746   IPI00916636   IPI00916813   IPI00915847   
Protein Interaction databases
DIP (DOE-UCLA)Q8TC57
IntAct (EBI)Q8TC57
FunCoupENSG00000159374
BioGRIDM1AP
STRING (EMBL)M1AP
ZODIACM1AP
Ontologies - Pathways
QuickGOQ8TC57
Ontology : AmiGOmolecular_function  protein binding  cytoplasm  RNA processing  spermatogenesis  female gamete generation  integral component of membrane  cell differentiation  chromatin assembly  male meiosis chromosome separation  
Ontology : EGO-EBImolecular_function  protein binding  cytoplasm  RNA processing  spermatogenesis  female gamete generation  integral component of membrane  cell differentiation  chromatin assembly  male meiosis chromosome separation  
NDEx NetworkM1AP
Atlas of Cancer Signalling NetworkM1AP
Wikipedia pathwaysM1AP
Orthology - Evolution
OrthoDB130951
GeneTree (enSembl)ENSG00000159374
Phylogenetic Trees/Animal Genes : TreeFamM1AP
HOVERGENQ8TC57
HOGENOMQ8TC57
Homologs : HomoloGeneM1AP
Homology/Alignments : Family Browser (UCSC)M1AP
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerM1AP [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)M1AP
dbVarM1AP
ClinVarM1AP
1000_GenomesM1AP 
Exome Variant ServerM1AP
ExAC (Exome Aggregation Consortium)M1AP (select the gene name)
Genetic variants : HAPMAP130951
Genomic Variants (DGV)M1AP [DGVbeta]
DECIPHER (Syndromes)2:74802387-74875465  ENSG00000159374
CONAN: Copy Number AnalysisM1AP 
Mutations
ICGC Data PortalM1AP 
TCGA Data PortalM1AP 
Broad Tumor PortalM1AP
OASIS PortalM1AP [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDM1AP
BioMutasearch M1AP
DgiDB (Drug Gene Interaction Database)M1AP
DoCM (Curated mutations)M1AP (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)M1AP (select a term)
intoGenM1AP
Cancer3DM1AP(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenM1AP
Genetic Testing Registry M1AP
NextProtQ8TC57 [Medical]
TSGene130951
GENETestsM1AP
Huge Navigator M1AP [HugePedia]
snp3D : Map Gene to Disease130951
BioCentury BCIQM1AP
ClinGenM1AP
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD130951
Chemical/Pharm GKB GenePA162379401
Clinical trialM1AP
Miscellaneous
canSAR (ICR)M1AP (select the gene name)
Probes
Litterature
PubMed10 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineM1AP
EVEXM1AP
GoPubMedM1AP
iHOPM1AP
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:27:30 CET 2017

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