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MORN4 (MORN repeat containing 4)

Identity

Alias (NCBI)C10orf83
UTA
bA548K23.4
rtp
HGNC (Hugo) MORN4
HGNC Alias symbbA548K23.4
FLJ25925
rtp
HGNC Alias name44050 protein
 retinophilin homolog (Drosophila)
HGNC Previous nameC10orf83
HGNC Previous namechromosome 10 open reading frame 83
LocusID (NCBI) 118812
Atlas_Id 70377
Location 10q24.2  [Link to chromosome band 10q24]
Location_base_pair Starts at 97614555 and ends at 97633500 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)
TBC1D12 (10q23.33) / MORN4 (10q24.2)

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)MORN4   24001
Cards
Entrez_Gene (NCBI)MORN4    MORN repeat containing 4
AliasesC10orf83; UTA; bA548K23.4; rtp
GeneCards (Weizmann)MORN4
Ensembl hg19 (Hinxton)ENSG00000171160 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000171160 [Gene_View]  ENSG00000171160 [Sequence]  chr10:97614555-97633500 [Contig_View]  MORN4 [Vega]
ICGC DataPortalENSG00000171160
TCGA cBioPortalMORN4
AceView (NCBI)MORN4
Genatlas (Paris)MORN4
SOURCE (Princeton)MORN4
Genetics Home Reference (NIH)MORN4
Genomic and cartography
GoldenPath hg38 (UCSC)MORN4  -     chr10:97614555-97633500 -  10q24.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MORN4  -     10q24.2   [Description]    (hg19-Feb_2009)
GoldenPathMORN4 - 10q24.2 [CytoView hg19]  MORN4 - 10q24.2 [CytoView hg38]
ImmunoBaseENSG00000171160
Genome Data Viewer NCBIMORN4 [Mapview hg19]  
OMIM617736   
Gene and transcription
Genbank (Entrez)AJ312050 AJ431726 AK098791 AK289406 AL834132
RefSeq transcript (Entrez)NM_001098831 NM_178832
Consensus coding sequences : CCDS (NCBI)MORN4
Gene ExpressionMORN4 [ NCBI-GEO ]   MORN4 [ EBI - ARRAY_EXPRESS ]   MORN4 [ SEEK ]   MORN4 [ MEM ]
Gene Expression Viewer (FireBrowse)MORN4 [ Firebrowse - Broad ]
GenevisibleExpression of MORN4 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)118812
GTEX Portal (Tissue expression)MORN4
Human Protein AtlasENSG00000171160-MORN4 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8NDC4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8NDC4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8NDC4
PhosPhoSitePlusQ8NDC4
Domains : Interpro (EBI)MORN   
Domain families : Pfam (Sanger)MORN (PF02493)   
Domain families : Pfam (NCBI)pfam02493   
Domain families : Smart (EMBL)MORN (SM00698)  
Conserved Domain (NCBI)MORN4
SuperfamilyQ8NDC4
AlphaFold pdb e-kbQ8NDC4   
Human Protein Atlas [tissue]ENSG00000171160-MORN4 [tissue]
HPRD16584
Protein Interaction databases
DIP (DOE-UCLA)Q8NDC4
IntAct (EBI)Q8NDC4
BioGRIDMORN4
STRING (EMBL)MORN4
ZODIACMORN4
Ontologies - Pathways
QuickGOQ8NDC4
Ontology : AmiGOprotein binding  cytoplasm  stereocilium tip  filopodium tip  response to axon injury  
Ontology : EGO-EBIprotein binding  cytoplasm  stereocilium tip  filopodium tip  response to axon injury  
NDEx NetworkMORN4
Atlas of Cancer Signalling NetworkMORN4
Wikipedia pathwaysMORN4
Orthology - Evolution
OrthoDB118812
GeneTree (enSembl)ENSG00000171160
Phylogenetic Trees/Animal Genes : TreeFamMORN4
Homologs : HomoloGeneMORN4
Homology/Alignments : Family Browser (UCSC)MORN4
Gene fusions - Rearrangements
Fusion : QuiverMORN4
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMORN4 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MORN4
dbVarMORN4
ClinVarMORN4
MonarchMORN4
1000_GenomesMORN4 
Exome Variant ServerMORN4
GNOMAD BrowserENSG00000171160
Varsome BrowserMORN4
ACMGMORN4 variants
VarityQ8NDC4
Genomic Variants (DGV)MORN4 [DGVbeta]
DECIPHERMORN4 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMORN4 
Mutations
ICGC Data PortalMORN4 
TCGA Data PortalMORN4 
Broad Tumor PortalMORN4
OASIS PortalMORN4 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMORN4  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DMORN4
Mutations and Diseases : HGMDMORN4
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaMORN4
DgiDB (Drug Gene Interaction Database)MORN4
DoCM (Curated mutations)MORN4
CIViC (Clinical Interpretations of Variants in Cancer)MORN4
Cancer3DMORN4
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM617736   
Orphanet
DisGeNETMORN4
MedgenMORN4
Genetic Testing Registry MORN4
NextProtQ8NDC4 [Medical]
GENETestsMORN4
Target ValidationMORN4
Huge Navigator MORN4 [HugePedia]
ClinGenMORN4
Clinical trials, drugs, therapy
MyCancerGenomeMORN4
Protein Interactions : CTDMORN4
Pharm GKB GenePA162396074
PharosQ8NDC4
Clinical trialMORN4
Miscellaneous
canSAR (ICR)MORN4
HarmonizomeMORN4
DataMed IndexMORN4
Probes
Litterature
PubMed13 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXMORN4
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Mon Oct 4 16:11:27 CEST 2021

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