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MORN2 (MORN repeat containing 2)

Identity

Alias_symbol (synonym)MOPT
Other aliasBLOCK27
HGNC (Hugo) MORN2
LocusID (NCBI) 729967
Atlas_Id 70375
Location 2p22.1  [Link to chromosome band 2p22]
Location_base_pair Starts at 38875962 and ends at 38882709 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)

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)MORN2   30166
Cards
Entrez_Gene (NCBI)MORN2  729967  MORN repeat containing 2
AliasesBLOCK27; MOPT
GeneCards (Weizmann)MORN2
Ensembl hg19 (Hinxton)ENSG00000188010 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000188010 [Gene_View]  chr2:38875962-38882709 [Contig_View]  MORN2 [Vega]
ICGC DataPortalENSG00000188010
TCGA cBioPortalMORN2
AceView (NCBI)MORN2
Genatlas (Paris)MORN2
WikiGenes729967
SOURCE (Princeton)MORN2
Genetics Home Reference (NIH)MORN2
Genomic and cartography
GoldenPath hg38 (UCSC)MORN2  -     chr2:38875962-38882709 +  2p22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MORN2  -     2p22.1   [Description]    (hg19-Feb_2009)
EnsemblMORN2 - 2p22.1 [CytoView hg19]  MORN2 - 2p22.1 [CytoView hg38]
Mapping of homologs : NCBIMORN2 [Mapview hg19]  MORN2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AY367766 BC095472 BC102032 BC102034 BC102035
RefSeq transcript (Entrez)NM_001145450 NM_194270
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MORN2
Cluster EST : UnigeneHs.729207 [ NCBI ]
CGAP (NCI)Hs.729207
Alternative Splicing GalleryENSG00000188010
Gene ExpressionMORN2 [ NCBI-GEO ]   MORN2 [ EBI - ARRAY_EXPRESS ]   MORN2 [ SEEK ]   MORN2 [ MEM ]
Gene Expression Viewer (FireBrowse)MORN2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)729967
GTEX Portal (Tissue expression)MORN2
Human Protein AtlasENSG00000188010-MORN2 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ502X0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ502X0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ502X0
Splice isoforms : SwissVarQ502X0
PhosPhoSitePlusQ502X0
Domains : Interpro (EBI)MORN   
Domain families : Pfam (Sanger)MORN (PF02493)   
Domain families : Pfam (NCBI)pfam02493   
Domain families : Smart (EMBL)MORN (SM00698)  
Conserved Domain (NCBI)MORN2
DMDM Disease mutations729967
Blocks (Seattle)MORN2
SuperfamilyQ502X0
Human Protein Atlas [tissue]ENSG00000188010-MORN2 [tissue]
Peptide AtlasQ502X0
IPIIPI00375562   IPI00917816   IPI00917007   IPI00915785   
Protein Interaction databases
DIP (DOE-UCLA)Q502X0
IntAct (EBI)Q502X0
FunCoupENSG00000188010
BioGRIDMORN2
STRING (EMBL)MORN2
ZODIACMORN2
Ontologies - Pathways
QuickGOQ502X0
Ontology : AmiGOacrosomal vesicle  protein binding  nucleus  spermatogenesis  cell differentiation  
Ontology : EGO-EBIacrosomal vesicle  protein binding  nucleus  spermatogenesis  cell differentiation  
NDEx NetworkMORN2
Atlas of Cancer Signalling NetworkMORN2
Wikipedia pathwaysMORN2
Orthology - Evolution
OrthoDB729967
GeneTree (enSembl)ENSG00000188010
Phylogenetic Trees/Animal Genes : TreeFamMORN2
HOVERGENQ502X0
HOGENOMQ502X0
Homologs : HomoloGeneMORN2
Homology/Alignments : Family Browser (UCSC)MORN2
Gene fusions - Rearrangements
Tumor Fusion PortalMORN2
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMORN2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MORN2
dbVarMORN2
ClinVarMORN2
1000_GenomesMORN2 
Exome Variant ServerMORN2
ExAC (Exome Aggregation Consortium)ENSG00000188010
GNOMAD BrowserENSG00000188010
Genetic variants : HAPMAP729967
Genomic Variants (DGV)MORN2 [DGVbeta]
DECIPHERMORN2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMORN2 
Mutations
ICGC Data PortalMORN2 
TCGA Data PortalMORN2 
Broad Tumor PortalMORN2
OASIS PortalMORN2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMORN2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMORN2
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch MORN2
DgiDB (Drug Gene Interaction Database)MORN2
DoCM (Curated mutations)MORN2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MORN2 (select a term)
intoGenMORN2
Cancer3DMORN2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETMORN2
MedgenMORN2
Genetic Testing Registry MORN2
NextProtQ502X0 [Medical]
TSGene729967
GENETestsMORN2
Target ValidationMORN2
Huge Navigator MORN2 [HugePedia]
snp3D : Map Gene to Disease729967
BioCentury BCIQMORN2
ClinGenMORN2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD729967
Chemical/Pharm GKB GenePA142671343
Clinical trialMORN2
Miscellaneous
canSAR (ICR)MORN2 (select the gene name)
Probes
Litterature
PubMed12 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMORN2
EVEXMORN2
GoPubMedMORN2
iHOPMORN2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Nov 21 13:05:47 CET 2017

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