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KLF14 (Kruppel like factor 14)

Identity

Alias_symbol (synonym)BTEB5
Other alias
HGNC (Hugo) KLF14
LocusID (NCBI) 136259
Atlas_Id 55760
Location 7q32.2  [Link to chromosome band 7q32]
Location_base_pair Starts at 130732554 and ends at 130734033 bp from pter ( according to hg38-Dec_2013)

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)KLF14   23025
LRG (Locus Reference Genomic)LRG_1039
Cards
Entrez_Gene (NCBI)KLF14  136259  Kruppel like factor 14
AliasesBTEB5
GeneCards (Weizmann)KLF14
Ensembl hg19 (Hinxton)ENSG00000266265 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266265 [Gene_View]  chr7:130732554-130734033 [Contig_View]  KLF14 [Vega]
ICGC DataPortalENSG00000266265
TCGA cBioPortalKLF14
AceView (NCBI)KLF14
Genatlas (Paris)KLF14
WikiGenes136259
SOURCE (Princeton)KLF14
Genetics Home Reference (NIH)KLF14
Genomic and cartography
GoldenPath hg38 (UCSC)KLF14  -     chr7:130732554-130734033 -  7q32.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)KLF14  -     7q32.2   [Description]    (hg19-Feb_2009)
EnsemblKLF14 - 7q32.2 [CytoView hg19]  KLF14 - 7q32.2 [CytoView hg38]
Mapping of homologs : NCBIKLF14 [Mapview hg19]  KLF14 [Mapview hg38]
OMIM609393   
Gene and transcription
Genbank (Entrez)AA455939 AF490374 BC160035 DQ534757
RefSeq transcript (Entrez)NM_138693
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)KLF14
Cluster EST : UnigeneHs.125240 [ NCBI ]
CGAP (NCI)Hs.125240
Alternative Splicing GalleryENSG00000266265
Gene ExpressionKLF14 [ NCBI-GEO ]   KLF14 [ EBI - ARRAY_EXPRESS ]   KLF14 [ SEEK ]   KLF14 [ MEM ]
Gene Expression Viewer (FireBrowse)KLF14 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)136259
GTEX Portal (Tissue expression)KLF14
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8TD94   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8TD94  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8TD94
Splice isoforms : SwissVarQ8TD94
PhosPhoSitePlusQ8TD94
Domaine pattern : Prosite (Expaxy)ZINC_FINGER_C2H2_1 (PS00028)    ZINC_FINGER_C2H2_2 (PS50157)   
Domains : Interpro (EBI)Znf_C2H2    Znf_C2H2-like    Znf_C2H2/integrase_DNA-bd   
Domain families : Pfam (Sanger)zf-C2H2 (PF00096)   
Domain families : Pfam (NCBI)pfam00096   
Domain families : Smart (EMBL)ZnF_C2H2 (SM00355)  
Conserved Domain (NCBI)KLF14
DMDM Disease mutations136259
Blocks (Seattle)KLF14
SuperfamilyQ8TD94
Human Protein AtlasENSG00000266265
Peptide AtlasQ8TD94
HPRD13919
IPIIPI00152493   
Protein Interaction databases
DIP (DOE-UCLA)Q8TD94
IntAct (EBI)Q8TD94
FunCoupENSG00000266265
BioGRIDKLF14
STRING (EMBL)KLF14
ZODIACKLF14
Ontologies - Pathways
QuickGOQ8TD94
Ontology : AmiGODNA binding  nucleus  transcription, DNA-templated  positive regulation of transcription from RNA polymerase II promoter  metal ion binding  
Ontology : EGO-EBIDNA binding  nucleus  transcription, DNA-templated  positive regulation of transcription from RNA polymerase II promoter  metal ion binding  
NDEx NetworkKLF14
Atlas of Cancer Signalling NetworkKLF14
Wikipedia pathwaysKLF14
Orthology - Evolution
OrthoDB136259
GeneTree (enSembl)ENSG00000266265
Phylogenetic Trees/Animal Genes : TreeFamKLF14
HOVERGENQ8TD94
HOGENOMQ8TD94
Homologs : HomoloGeneKLF14
Homology/Alignments : Family Browser (UCSC)KLF14
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKLF14 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KLF14
dbVarKLF14
ClinVarKLF14
1000_GenomesKLF14 
Exome Variant ServerKLF14
ExAC (Exome Aggregation Consortium)KLF14 (select the gene name)
Genetic variants : HAPMAP136259
Genomic Variants (DGV)KLF14 [DGVbeta]
DECIPHERKLF14 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisKLF14 
Mutations
ICGC Data PortalKLF14 
TCGA Data PortalKLF14 
Broad Tumor PortalKLF14
OASIS PortalKLF14 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKLF14  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDKLF14
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 KLF14
DgiDB (Drug Gene Interaction Database)KLF14
DoCM (Curated mutations)KLF14 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KLF14 (select a term)
intoGenKLF14
Cancer3DKLF14(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM609393   
Orphanet
MedgenKLF14
Genetic Testing Registry KLF14
NextProtQ8TD94 [Medical]
TSGene136259
GENETestsKLF14
Target ValidationKLF14
Huge Navigator KLF14 [HugePedia]
snp3D : Map Gene to Disease136259
BioCentury BCIQKLF14
ClinGenKLF14 (curated)
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD136259
Chemical/Pharm GKB GenePA134868089
Clinical trialKLF14
Miscellaneous
canSAR (ICR)KLF14 (select the gene name)
Probes
Litterature
PubMed23 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKLF14
EVEXKLF14
GoPubMedKLF14
iHOPKLF14
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed Jun 7 12:39:44 CEST 2017

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