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SLC16A14 (solute carrier family 16 member 14)

Identity

Alias_namessolute carrier family 16 (monocarboxylic acid transporters), member 14
solute carrier family 16, member 14
Alias_symbol (synonym)FLJ30794
MCT14
Other alias
HGNC (Hugo) SLC16A14
LocusID (NCBI) 151473
Atlas_Id 73293
Location 2q36.3  [Link to chromosome band 2q36]
Location_base_pair Starts at 230034974 and ends at 230068999 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
SLC16A14 (2q36.3) / SP110 (2q37.1)TRIP12 (2q36.3) / SLC16A14 (2q36.3)

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)SLC16A14   26417
Cards
Entrez_Gene (NCBI)SLC16A14  151473  solute carrier family 16 member 14
AliasesMCT14
GeneCards (Weizmann)SLC16A14
Ensembl hg19 (Hinxton)ENSG00000163053 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000163053 [Gene_View]  chr2:230034974-230068999 [Contig_View]  SLC16A14 [Vega]
ICGC DataPortalENSG00000163053
TCGA cBioPortalSLC16A14
AceView (NCBI)SLC16A14
Genatlas (Paris)SLC16A14
WikiGenes151473
SOURCE (Princeton)SLC16A14
Genetics Home Reference (NIH)SLC16A14
Genomic and cartography
GoldenPath hg38 (UCSC)SLC16A14  -     chr2:230034974-230068999 -  2q36.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SLC16A14  -     2q36.3   [Description]    (hg19-Feb_2009)
EnsemblSLC16A14 - 2q36.3 [CytoView hg19]  SLC16A14 - 2q36.3 [CytoView hg38]
Mapping of homologs : NCBISLC16A14 [Mapview hg19]  SLC16A14 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK055317 AK055356 AK123207 AK292873 AL833470
RefSeq transcript (Entrez)NM_152527
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SLC16A14
Cluster EST : UnigeneHs.504317 [ NCBI ]
CGAP (NCI)Hs.504317
Alternative Splicing GalleryENSG00000163053
Gene ExpressionSLC16A14 [ NCBI-GEO ]   SLC16A14 [ EBI - ARRAY_EXPRESS ]   SLC16A14 [ SEEK ]   SLC16A14 [ MEM ]
Gene Expression Viewer (FireBrowse)SLC16A14 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)151473
GTEX Portal (Tissue expression)SLC16A14
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ7RTX9   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ7RTX9  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ7RTX9
Splice isoforms : SwissVarQ7RTX9
PhosPhoSitePlusQ7RTX9
Domaine pattern : Prosite (Expaxy)MFS (PS50850)   
Domains : Interpro (EBI)MFS    MFS_dom   
Domain families : Pfam (Sanger)MFS_1 (PF07690)   
Domain families : Pfam (NCBI)pfam07690   
Conserved Domain (NCBI)SLC16A14
DMDM Disease mutations151473
Blocks (Seattle)SLC16A14
SuperfamilyQ7RTX9
Human Protein AtlasENSG00000163053
Peptide AtlasQ7RTX9
HPRD15347
IPIIPI00043689   IPI00847918   IPI00807510   IPI00916878   IPI00917021   IPI00916583   
Protein Interaction databases
DIP (DOE-UCLA)Q7RTX9
IntAct (EBI)Q7RTX9
FunCoupENSG00000163053
BioGRIDSLC16A14
STRING (EMBL)SLC16A14
ZODIACSLC16A14
Ontologies - Pathways
QuickGOQ7RTX9
Ontology : AmiGOplasma membrane  symporter activity  integral component of membrane  transmembrane transport  
Ontology : EGO-EBIplasma membrane  symporter activity  integral component of membrane  transmembrane transport  
NDEx NetworkSLC16A14
Atlas of Cancer Signalling NetworkSLC16A14
Wikipedia pathwaysSLC16A14
Orthology - Evolution
OrthoDB151473
GeneTree (enSembl)ENSG00000163053
Phylogenetic Trees/Animal Genes : TreeFamSLC16A14
HOVERGENQ7RTX9
HOGENOMQ7RTX9
Homologs : HomoloGeneSLC16A14
Homology/Alignments : Family Browser (UCSC)SLC16A14
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerSLC16A14 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)SLC16A14
dbVarSLC16A14
ClinVarSLC16A14
1000_GenomesSLC16A14 
Exome Variant ServerSLC16A14
ExAC (Exome Aggregation Consortium)SLC16A14 (select the gene name)
Genetic variants : HAPMAP151473
Genomic Variants (DGV)SLC16A14 [DGVbeta]
DECIPHERSLC16A14 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisSLC16A14 
Mutations
ICGC Data PortalSLC16A14 
TCGA Data PortalSLC16A14 
Broad Tumor PortalSLC16A14
OASIS PortalSLC16A14 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICSLC16A14  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDSLC16A14
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 SLC16A14
DgiDB (Drug Gene Interaction Database)SLC16A14
DoCM (Curated mutations)SLC16A14 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)SLC16A14 (select a term)
intoGenSLC16A14
Cancer3DSLC16A14(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenSLC16A14
Genetic Testing Registry SLC16A14
NextProtQ7RTX9 [Medical]
TSGene151473
GENETestsSLC16A14
Target ValidationSLC16A14
Huge Navigator SLC16A14 [HugePedia]
snp3D : Map Gene to Disease151473
BioCentury BCIQSLC16A14
ClinGenSLC16A14
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD151473
Chemical/Pharm GKB GenePA134983567
Clinical trialSLC16A14
Miscellaneous
canSAR (ICR)SLC16A14 (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSLC16A14
EVEXSLC16A14
GoPubMedSLC16A14
iHOPSLC16A14
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed May 31 15:40:53 CEST 2017

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