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SFXN2 (sideroflexin 2)

Identity

Alias (NCBI)SLC56A2
HGNC (Hugo) SFXN2
LocusID (NCBI) 118980
Atlas_Id 73174
Location 10q24.32  [Link to chromosome band 10q24]
Location_base_pair Starts at 102714636 and ends at 102743492 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)
UBXN2B (8q12.1) / SFXN2 (10q24.32)

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)SFXN2   16086
Cards
Entrez_Gene (NCBI)SFXN2    sideroflexin 2
AliasesSLC56A2
GeneCards (Weizmann)SFXN2
Ensembl hg19 (Hinxton)ENSG00000156398 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000156398 [Gene_View]  ENSG00000156398 [Sequence]  chr10:102714636-102743492 [Contig_View]  SFXN2 [Vega]
ICGC DataPortalENSG00000156398
TCGA cBioPortalSFXN2
AceView (NCBI)SFXN2
Genatlas (Paris)SFXN2
SOURCE (Princeton)SFXN2
Genetics Home Reference (NIH)SFXN2
Genomic and cartography
GoldenPath hg38 (UCSC)SFXN2  -     chr10:102714636-102743492 +  10q24.32   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SFXN2  -     10q24.32   [Description]    (hg19-Feb_2009)
GoldenPathSFXN2 - 10q24.32 [CytoView hg19]  SFXN2 - 10q24.32 [CytoView hg38]
ImmunoBaseENSG00000156398
Genome Data Viewer NCBISFXN2 [Mapview hg19]  
OMIM615570   
Gene and transcription
Genbank (Entrez)AF462052 AK055711 AK308246 BC022091 BP871592
RefSeq transcript (Entrez)NM_001350989 NM_178858
Consensus coding sequences : CCDS (NCBI)SFXN2
Gene ExpressionSFXN2 [ NCBI-GEO ]   SFXN2 [ EBI - ARRAY_EXPRESS ]   SFXN2 [ SEEK ]   SFXN2 [ MEM ]
Gene Expression Viewer (FireBrowse)SFXN2 [ Firebrowse - Broad ]
GenevisibleExpression of SFXN2 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)118980
GTEX Portal (Tissue expression)SFXN2
Human Protein AtlasENSG00000156398-SFXN2 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96NB2   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96NB2  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96NB2
PhosPhoSitePlusQ96NB2
Domains : Interpro (EBI)Mtc   
Domain families : Pfam (Sanger)SFXNs (PF03820)   
Domain families : Pfam (NCBI)pfam03820   
Conserved Domain (NCBI)SFXN2
SuperfamilyQ96NB2
AlphaFold pdb e-kbQ96NB2   
Human Protein Atlas [tissue]ENSG00000156398-SFXN2 [tissue]
HPRD18045
Protein Interaction databases
DIP (DOE-UCLA)Q96NB2
IntAct (EBI)Q96NB2
BioGRIDSFXN2
STRING (EMBL)SFXN2
ZODIACSFXN2
Ontologies - Pathways
QuickGOQ96NB2
Ontology : AmiGOprotein binding  mitochondrion  transmembrane transporter activity  serine transmembrane transporter activity  integral component of mitochondrial inner membrane  serine import into mitochondrion  mitochondrial transmembrane transport  mitochondrial transmembrane transport  
Ontology : EGO-EBIprotein binding  mitochondrion  transmembrane transporter activity  serine transmembrane transporter activity  integral component of mitochondrial inner membrane  serine import into mitochondrion  mitochondrial transmembrane transport  mitochondrial transmembrane transport  
NDEx NetworkSFXN2
Atlas of Cancer Signalling NetworkSFXN2
Wikipedia pathwaysSFXN2
Orthology - Evolution
OrthoDB118980
GeneTree (enSembl)ENSG00000156398
Phylogenetic Trees/Animal Genes : TreeFamSFXN2
Homologs : HomoloGeneSFXN2
Homology/Alignments : Family Browser (UCSC)SFXN2
Gene fusions - Rearrangements
Fusion : QuiverSFXN2
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerSFXN2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)SFXN2
dbVarSFXN2
ClinVarSFXN2
MonarchSFXN2
1000_GenomesSFXN2 
Exome Variant ServerSFXN2
GNOMAD BrowserENSG00000156398
Varsome BrowserSFXN2
ACMGSFXN2 variants
VarityQ96NB2
Genomic Variants (DGV)SFXN2 [DGVbeta]
DECIPHERSFXN2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisSFXN2 
Mutations
ICGC Data PortalSFXN2 
TCGA Data PortalSFXN2 
Broad Tumor PortalSFXN2
OASIS PortalSFXN2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICSFXN2  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DSFXN2
Mutations and Diseases : HGMDSFXN2
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaSFXN2
DgiDB (Drug Gene Interaction Database)SFXN2
DoCM (Curated mutations)SFXN2
CIViC (Clinical Interpretations of Variants in Cancer)SFXN2
Cancer3DSFXN2
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM615570   
Orphanet
DisGeNETSFXN2
MedgenSFXN2
Genetic Testing Registry SFXN2
NextProtQ96NB2 [Medical]
GENETestsSFXN2
Target ValidationSFXN2
Huge Navigator SFXN2 [HugePedia]
ClinGenSFXN2
Clinical trials, drugs, therapy
MyCancerGenomeSFXN2
Protein Interactions : CTDSFXN2
Pharm GKB GenePA38091
PharosQ96NB2
Clinical trialSFXN2
Miscellaneous
canSAR (ICR)SFXN2
HarmonizomeSFXN2
DataMed IndexSFXN2
Probes
Litterature
PubMed30 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXSFXN2
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 16:20:22 CEST 2021

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