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MORN5 (MORN repeat containing 5)

Identity

Alias_namesC9orf113
C9orf18
chromosome 9 open reading frame 113
chromosome 9 open reading frame 18
Alias_symbol (synonym)FLJ46909
Other alias
HGNC (Hugo) MORN5
LocusID (NCBI) 254956
Atlas_Id 70378
Location 9q33.2  [Link to chromosome band 9q33]
Location_base_pair Starts at 122159908 and ends at 122200088 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
MRRF (9q33.2) / MORN5 (9q33.2)

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)MORN5   17841
Cards
Entrez_Gene (NCBI)MORN5  254956  MORN repeat containing 5
AliasesC9orf113; C9orf18
GeneCards (Weizmann)MORN5
Ensembl hg19 (Hinxton)ENSG00000185681 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000185681 [Gene_View]  chr9:122159908-122200088 [Contig_View]  MORN5 [Vega]
ICGC DataPortalENSG00000185681
TCGA cBioPortalMORN5
AceView (NCBI)MORN5
Genatlas (Paris)MORN5
WikiGenes254956
SOURCE (Princeton)MORN5
Genetics Home Reference (NIH)MORN5
Genomic and cartography
GoldenPath hg38 (UCSC)MORN5  -     chr9:122159908-122200088 +  9q33.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MORN5  -     9q33.2   [Description]    (hg19-Feb_2009)
EnsemblMORN5 - 9q33.2 [CytoView hg19]  MORN5 - 9q33.2 [CytoView hg38]
Mapping of homologs : NCBIMORN5 [Mapview hg19]  MORN5 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI026684 AI560944 AK128877 AK302081 BC133690
RefSeq transcript (Entrez)NM_001286828 NM_198469
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MORN5
Cluster EST : UnigeneHs.71428 [ NCBI ]
CGAP (NCI)Hs.71428
Alternative Splicing GalleryENSG00000185681
Gene ExpressionMORN5 [ NCBI-GEO ]   MORN5 [ EBI - ARRAY_EXPRESS ]   MORN5 [ SEEK ]   MORN5 [ MEM ]
Gene Expression Viewer (FireBrowse)MORN5 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)254956
GTEX Portal (Tissue expression)MORN5
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5VZ52   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5VZ52  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5VZ52
Splice isoforms : SwissVarQ5VZ52
PhosPhoSitePlusQ5VZ52
Domains : Interpro (EBI)MORN   
Domain families : Pfam (Sanger)MORN (PF02493)   
Domain families : Pfam (NCBI)pfam02493   
Domain families : Smart (EMBL)MORN (SM00698)  
Conserved Domain (NCBI)MORN5
DMDM Disease mutations254956
Blocks (Seattle)MORN5
SuperfamilyQ5VZ52
Human Protein AtlasENSG00000185681
Peptide AtlasQ5VZ52
HPRD12947
IPIIPI00394817   IPI00922345   IPI00640336   
Protein Interaction databases
DIP (DOE-UCLA)Q5VZ52
IntAct (EBI)Q5VZ52
FunCoupENSG00000185681
BioGRIDMORN5
STRING (EMBL)MORN5
ZODIACMORN5
Ontologies - Pathways
QuickGOQ5VZ52
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkMORN5
Atlas of Cancer Signalling NetworkMORN5
Wikipedia pathwaysMORN5
Orthology - Evolution
OrthoDB254956
GeneTree (enSembl)ENSG00000185681
Phylogenetic Trees/Animal Genes : TreeFamMORN5
HOVERGENQ5VZ52
HOGENOMQ5VZ52
Homologs : HomoloGeneMORN5
Homology/Alignments : Family Browser (UCSC)MORN5
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMORN5 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MORN5
dbVarMORN5
ClinVarMORN5
1000_GenomesMORN5 
Exome Variant ServerMORN5
ExAC (Exome Aggregation Consortium)MORN5 (select the gene name)
Genetic variants : HAPMAP254956
Genomic Variants (DGV)MORN5 [DGVbeta]
DECIPHERMORN5 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMORN5 
Mutations
ICGC Data PortalMORN5 
TCGA Data PortalMORN5 
Broad Tumor PortalMORN5
OASIS PortalMORN5 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMORN5  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMORN5
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch MORN5
DgiDB (Drug Gene Interaction Database)MORN5
DoCM (Curated mutations)MORN5 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MORN5 (select a term)
intoGenMORN5
Cancer3DMORN5(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMORN5
Genetic Testing Registry MORN5
NextProtQ5VZ52 [Medical]
TSGene254956
GENETestsMORN5
Target ValidationMORN5
Huge Navigator MORN5 [HugePedia]
snp3D : Map Gene to Disease254956
BioCentury BCIQMORN5
ClinGenMORN5
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD254956
Chemical/Pharm GKB GenePA25975
Clinical trialMORN5
Miscellaneous
canSAR (ICR)MORN5 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMORN5
EVEXMORN5
GoPubMedMORN5
iHOPMORN5
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:31:01 CEST 2017

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