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MFSD6L (major facilitator superfamily domain containing 6-like)

Identity

Alias_namesmajor facilitator superfamily domain containing 6-like
Alias_symbol (synonym)FLJ35773
Other alias-
HGNC (Hugo) MFSD6L
LocusID (NCBI) 162387
Atlas_Id 68945
Location 17p13.1  [Link to chromosome band 17p13]
Location_base_pair Starts at 8700428 and ends at 8702667 bp from pter ( according to hg19-Feb_2009)

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)MFSD6L   26656
Cards
Entrez_Gene (NCBI)MFSD6L  162387  major facilitator superfamily domain containing 6-like
Aliases
GeneCards (Weizmann)MFSD6L
Ensembl hg19 (Hinxton)ENSG00000185156 [Gene_View]  chr17:8700428-8702667 [Contig_View]  MFSD6L [Vega]
Ensembl hg38 (Hinxton)ENSG00000185156 [Gene_View]  chr17:8700428-8702667 [Contig_View]  MFSD6L [Vega]
ICGC DataPortalENSG00000185156
TCGA cBioPortalMFSD6L
AceView (NCBI)MFSD6L
Genatlas (Paris)MFSD6L
WikiGenes162387
SOURCE (Princeton)MFSD6L
Genetics Home Reference (NIH)MFSD6L
Genomic and cartography
GoldenPath hg19 (UCSC)MFSD6L  -     chr17:8700428-8702667 -  17p13.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MFSD6L  -     17p13.1   [Description]    (hg38-Dec_2013)
EnsemblMFSD6L - 17p13.1 [CytoView hg19]  MFSD6L - 17p13.1 [CytoView hg38]
Mapping of homologs : NCBIMFSD6L [Mapview hg19]  MFSD6L [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK093092 AY129026 BC040487 BM986935
RefSeq transcript (Entrez)NM_152599
RefSeq genomic (Entrez)NC_000017 NC_018928 NT_010718 NW_004929405
Consensus coding sequences : CCDS (NCBI)MFSD6L
Cluster EST : UnigeneHs.213603 [ NCBI ]
CGAP (NCI)Hs.213603
Alternative Splicing GalleryENSG00000185156
Gene ExpressionMFSD6L [ NCBI-GEO ]   MFSD6L [ EBI - ARRAY_EXPRESS ]   MFSD6L [ SEEK ]   MFSD6L [ MEM ]
Gene Expression Viewer (FireBrowse)MFSD6L [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)162387
GTEX Portal (Tissue expression)MFSD6L
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8IWD5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8IWD5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8IWD5
Splice isoforms : SwissVarQ8IWD5
PhosPhoSitePlusQ8IWD5
Domains : Interpro (EBI)MFS_dom   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MFSD6L
DMDM Disease mutations162387
Blocks (Seattle)MFSD6L
SuperfamilyQ8IWD5
Human Protein AtlasENSG00000185156
Peptide AtlasQ8IWD5
HPRD08186
IPIIPI00293085   
Protein Interaction databases
DIP (DOE-UCLA)Q8IWD5
IntAct (EBI)Q8IWD5
FunCoupENSG00000185156
BioGRIDMFSD6L
STRING (EMBL)MFSD6L
ZODIACMFSD6L
Ontologies - Pathways
QuickGOQ8IWD5
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkMFSD6L
Atlas of Cancer Signalling NetworkMFSD6L
Wikipedia pathwaysMFSD6L
Orthology - Evolution
OrthoDB162387
GeneTree (enSembl)ENSG00000185156
Phylogenetic Trees/Animal Genes : TreeFamMFSD6L
HOVERGENQ8IWD5
HOGENOMQ8IWD5
Homologs : HomoloGeneMFSD6L
Homology/Alignments : Family Browser (UCSC)MFSD6L
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMFSD6L [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MFSD6L
dbVarMFSD6L
ClinVarMFSD6L
1000_GenomesMFSD6L 
Exome Variant ServerMFSD6L
ExAC (Exome Aggregation Consortium)MFSD6L (select the gene name)
Genetic variants : HAPMAP162387
Genomic Variants (DGV)MFSD6L [DGVbeta]
DECIPHER (Syndromes)17:8700428-8702667  ENSG00000185156
CONAN: Copy Number AnalysisMFSD6L 
Mutations
ICGC Data PortalMFSD6L 
TCGA Data PortalMFSD6L 
Broad Tumor PortalMFSD6L
OASIS PortalMFSD6L [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMFSD6L  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMFSD6L
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 MFSD6L
DgiDB (Drug Gene Interaction Database)MFSD6L
DoCM (Curated mutations)MFSD6L (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MFSD6L (select a term)
intoGenMFSD6L
Cancer3DMFSD6L(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMFSD6L
Genetic Testing Registry MFSD6L
NextProtQ8IWD5 [Medical]
TSGene162387
GENETestsMFSD6L
Huge Navigator MFSD6L [HugePedia]
snp3D : Map Gene to Disease162387
BioCentury BCIQMFSD6L
ClinGenMFSD6L
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD162387
Chemical/Pharm GKB GenePA164722299
Clinical trialMFSD6L
Miscellaneous
canSAR (ICR)MFSD6L (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMFSD6L
EVEXMFSD6L
GoPubMedMFSD6L
iHOPMFSD6L
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:28:12 CET 2017

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