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MFSD14B (major facilitator superfamily domain containing 14B)

Identity

Alias (NCBI)HIATL1
HGNC (Hugo) MFSD14B
HGNC Alias symbFLJ14753
HGNC Previous nameHIATL1
HGNC Previous namehippocampus abundant transcript-like 1
LocusID (NCBI) 84641
Atlas_Id 56921
Location 9q22.32  [Link to chromosome band 9q22]
Location_base_pair Starts at 94374569 and ends at 94461037 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)
MFSD14B (9q22.32) / MFSD14B (9q22.32)MFSD14B (9q22.32) / SF3B1 (2q33.1)MFSD14B (9q22.32) / SH3GLB1 (1p22.3)

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)MFSD14B   23376
Cards
Entrez_Gene (NCBI)MFSD14B    major facilitator superfamily domain containing 14B
AliasesHIATL1
GeneCards (Weizmann)MFSD14B
Ensembl hg19 (Hinxton)ENSG00000148110 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000148110 [Gene_View]  ENSG00000148110 [Sequence]  chr9:94374569-94461037 [Contig_View]  MFSD14B [Vega]
ICGC DataPortalENSG00000148110
TCGA cBioPortalMFSD14B
AceView (NCBI)MFSD14B
Genatlas (Paris)MFSD14B
SOURCE (Princeton)MFSD14B
Genetics Home Reference (NIH)MFSD14B
Genomic and cartography
GoldenPath hg38 (UCSC)MFSD14B  -     chr9:94374569-94461037 +  9q22.32   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MFSD14B  -     9q22.32   [Description]    (hg19-Feb_2009)
GoldenPathMFSD14B - 9q22.32 [CytoView hg19]  MFSD14B - 9q22.32 [CytoView hg38]
ImmunoBaseENSG00000148110
Genome Data Viewer NCBIMFSD14B [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AF255650 AK027659 AK222836 AK300615 AL832415
RefSeq transcript (Entrez)NM_032558
Consensus coding sequences : CCDS (NCBI)MFSD14B
Gene ExpressionMFSD14B [ NCBI-GEO ]   MFSD14B [ EBI - ARRAY_EXPRESS ]   MFSD14B [ SEEK ]   MFSD14B [ MEM ]
Gene Expression Viewer (FireBrowse)MFSD14B [ Firebrowse - Broad ]
GenevisibleExpression of MFSD14B in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)84641
GTEX Portal (Tissue expression)MFSD14B
Human Protein AtlasENSG00000148110-MFSD14B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5SR56   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5SR56  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5SR56
PhosPhoSitePlusQ5SR56
Domaine pattern : Prosite (Expaxy)MFS (PS50850)    SUGAR_TRANSPORT_1 (PS00216)   
Domains : Interpro (EBI)MFS    MFS_dom    MFS_trans_sf    Sugar_transporter_CS    Tet-R_TetA/multi-R_MdtG   
Domain families : Pfam (Sanger)MFS_1 (PF07690)   
Domain families : Pfam (NCBI)pfam07690   
Conserved Domain (NCBI)MFSD14B
SuperfamilyQ5SR56
AlphaFold pdb e-kbQ5SR56   
Human Protein Atlas [tissue]ENSG00000148110-MFSD14B [tissue]
Protein Interaction databases
DIP (DOE-UCLA)Q5SR56
IntAct (EBI)Q5SR56
BioGRIDMFSD14B
STRING (EMBL)MFSD14B
ZODIACMFSD14B
Ontologies - Pathways
QuickGOQ5SR56
Ontology : AmiGOprotein binding  integral component of membrane  transmembrane transporter activity  transmembrane transport  
Ontology : EGO-EBIprotein binding  integral component of membrane  transmembrane transporter activity  transmembrane transport  
NDEx NetworkMFSD14B
Atlas of Cancer Signalling NetworkMFSD14B
Wikipedia pathwaysMFSD14B
Orthology - Evolution
OrthoDB84641
GeneTree (enSembl)ENSG00000148110
Phylogenetic Trees/Animal Genes : TreeFamMFSD14B
Homologs : HomoloGeneMFSD14B
Homology/Alignments : Family Browser (UCSC)MFSD14B
Gene fusions - Rearrangements
Fusion : QuiverMFSD14B
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMFSD14B [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MFSD14B
dbVarMFSD14B
ClinVarMFSD14B
MonarchMFSD14B
1000_GenomesMFSD14B 
Exome Variant ServerMFSD14B
GNOMAD BrowserENSG00000148110
Varsome BrowserMFSD14B
ACMGMFSD14B variants
VarityQ5SR56
Genomic Variants (DGV)MFSD14B [DGVbeta]
DECIPHERMFSD14B [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMFSD14B 
Mutations
ICGC Data PortalMFSD14B 
TCGA Data PortalMFSD14B 
Broad Tumor PortalMFSD14B
OASIS PortalMFSD14B [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMFSD14B  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DMFSD14B
Mutations and Diseases : HGMDMFSD14B
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaMFSD14B
DgiDB (Drug Gene Interaction Database)MFSD14B
DoCM (Curated mutations)MFSD14B
CIViC (Clinical Interpretations of Variants in Cancer)MFSD14B
Cancer3DMFSD14B
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETMFSD14B
MedgenMFSD14B
Genetic Testing Registry MFSD14B
NextProtQ5SR56 [Medical]
GENETestsMFSD14B
Target ValidationMFSD14B
Huge Navigator MFSD14B [HugePedia]
ClinGenMFSD14B
Clinical trials, drugs, therapy
MyCancerGenomeMFSD14B
Protein Interactions : CTDMFSD14B
Pharm GKB GenePA142671691
PharosQ5SR56
Clinical trialMFSD14B
Miscellaneous
canSAR (ICR)MFSD14B
HarmonizomeMFSD14B
DataMed IndexMFSD14B
Probes
Litterature
PubMed12 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXMFSD14B
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 15:18:25 CEST 2021

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