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NXF3 (nuclear RNA export factor 3)

Identity

Alias (NCBI)-
HGNC (Hugo) NXF3
LocusID (NCBI) 56000
Atlas_Id 47228
Location Xq22.1  [Link to chromosome band Xq22]
Location_base_pair Starts at 103075811 and ends at 103093143 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)
NXF3 (Xq22.1) / GOLGA8A (15q14)RNF44 (5q35.2) / NXF3 (Xq22.1)RNF44 5q35.2 / NXF3 Xq22.1

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)NXF3   8073
Cards
Entrez_Gene (NCBI)NXF3    nuclear RNA export factor 3
Aliases
GeneCards (Weizmann)NXF3
Ensembl hg19 (Hinxton)ENSG00000147206 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000147206 [Gene_View]  ENSG00000147206 [Sequence]  chrX:103075811-103093143 [Contig_View]  NXF3 [Vega]
ICGC DataPortalENSG00000147206
TCGA cBioPortalNXF3
AceView (NCBI)NXF3
Genatlas (Paris)NXF3
SOURCE (Princeton)NXF3
Genetics Home Reference (NIH)NXF3
Genomic and cartography
GoldenPath hg38 (UCSC)NXF3  -     chrX:103075811-103093143 -  Xq22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)NXF3  -     Xq22.1   [Description]    (hg19-Feb_2009)
GoldenPathNXF3 - Xq22.1 [CytoView hg19]  NXF3 - Xq22.1 [CytoView hg38]
ImmunoBaseENSG00000147206
Genome Data Viewer NCBINXF3 [Mapview hg19]  
OMIM300316   
Gene and transcription
Genbank (Entrez)AF346619 AJ277527 AJ277660 AK057086 AK294826
RefSeq transcript (Entrez)NM_022052
Consensus coding sequences : CCDS (NCBI)NXF3
Gene ExpressionNXF3 [ NCBI-GEO ]   NXF3 [ EBI - ARRAY_EXPRESS ]   NXF3 [ SEEK ]   NXF3 [ MEM ]
Gene Expression Viewer (FireBrowse)NXF3 [ Firebrowse - Broad ]
GenevisibleExpression of NXF3 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)56000
GTEX Portal (Tissue expression)NXF3
Human Protein AtlasENSG00000147206-NXF3 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9H4D5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9H4D5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9H4D5
PhosPhoSitePlusQ9H4D5
Domaine pattern : Prosite (Expaxy)NTF2_DOMAIN (PS50177)   
Domains : Interpro (EBI)LRR_dom_sf    NTF2    NTF2-like_dom_sf    Nuclear_transport_factor_2_euk    Nucleotide-bd_a/b_plait_sf    NXF3    NXF_fam    RBD_domain_sf    Tap_RNA-bd   
Domain families : Pfam (Sanger)NTF2 (PF02136)    Tap-RNA_bind (PF09162)   
Domain families : Pfam (NCBI)pfam02136    pfam09162   
Conserved Domain (NCBI)NXF3
SuperfamilyQ9H4D5
AlphaFold pdb e-kbQ9H4D5   
Human Protein Atlas [tissue]ENSG00000147206-NXF3 [tissue]
HPRD02261
Protein Interaction databases
DIP (DOE-UCLA)Q9H4D5
IntAct (EBI)Q9H4D5
BioGRIDNXF3
STRING (EMBL)NXF3
ZODIACNXF3
Ontologies - Pathways
QuickGOQ9H4D5
Ontology : AmiGORNA binding  mRNA binding  protein binding  nucleus  nucleus  nucleoplasm  cytoplasm  mRNA export from nucleus  poly(A)+ mRNA export from nucleus  nuclear RNA export factor complex  
Ontology : EGO-EBIRNA binding  mRNA binding  protein binding  nucleus  nucleus  nucleoplasm  cytoplasm  mRNA export from nucleus  poly(A)+ mRNA export from nucleus  nuclear RNA export factor complex  
Pathways : KEGGRibosome biogenesis in eukaryotes    RNA transport    mRNA surveillance pathway    Influenza A    Herpes simplex infection   
NDEx NetworkNXF3
Atlas of Cancer Signalling NetworkNXF3
Wikipedia pathwaysNXF3
Orthology - Evolution
OrthoDB56000
GeneTree (enSembl)ENSG00000147206
Phylogenetic Trees/Animal Genes : TreeFamNXF3
Homologs : HomoloGeneNXF3
Homology/Alignments : Family Browser (UCSC)NXF3
Gene fusions - Rearrangements
Fusion : MitelmanRNF44/NXF3 [5q35.2/Xq22.1]  
Fusion : QuiverNXF3
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerNXF3 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)NXF3
dbVarNXF3
ClinVarNXF3
MonarchNXF3
1000_GenomesNXF3 
Exome Variant ServerNXF3
GNOMAD BrowserENSG00000147206
Varsome BrowserNXF3
ACMGNXF3 variants
VarityQ9H4D5
Genomic Variants (DGV)NXF3 [DGVbeta]
DECIPHERNXF3 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisNXF3 
Mutations
ICGC Data PortalNXF3 
TCGA Data PortalNXF3 
Broad Tumor PortalNXF3
OASIS PortalNXF3 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICNXF3  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DNXF3
Mutations and Diseases : HGMDNXF3
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaNXF3
DgiDB (Drug Gene Interaction Database)NXF3
DoCM (Curated mutations)NXF3
CIViC (Clinical Interpretations of Variants in Cancer)NXF3
Cancer3DNXF3
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM300316   
Orphanet
DisGeNETNXF3
MedgenNXF3
Genetic Testing Registry NXF3
NextProtQ9H4D5 [Medical]
GENETestsNXF3
Target ValidationNXF3
Huge Navigator NXF3 [HugePedia]
ClinGenNXF3
Clinical trials, drugs, therapy
MyCancerGenomeNXF3
Protein Interactions : CTDNXF3
Pharm GKB GenePA31860
PharosQ9H4D5
Clinical trialNXF3
Miscellaneous
canSAR (ICR)NXF3
HarmonizomeNXF3
DataMed IndexNXF3
Probes
Litterature
PubMed17 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXNXF3
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:23:36 CEST 2021

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