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KLF8 (Kruppel-like factor 8)

Identity

Alias_symbol (synonym)BKLF3
ZNF741
DXS741
Other alias
HGNC (Hugo) KLF8
LocusID (NCBI) 11279
Atlas_Id 43804
Location Xp11.21  [Link to chromosome band Xp11]
Location_base_pair Starts at 56258870 and ends at 56314322 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)KLF8   6351
Cards
Entrez_Gene (NCBI)KLF8  11279  Kruppel-like factor 8
AliasesBKLF3; ZNF741
GeneCards (Weizmann)KLF8
Ensembl hg19 (Hinxton)ENSG00000102349 [Gene_View]  chrX:56258870-56314322 [Contig_View]  KLF8 [Vega]
Ensembl hg38 (Hinxton)ENSG00000102349 [Gene_View]  chrX:56258870-56314322 [Contig_View]  KLF8 [Vega]
ICGC DataPortalENSG00000102349
TCGA cBioPortalKLF8
AceView (NCBI)KLF8
Genatlas (Paris)KLF8
WikiGenes11279
SOURCE (Princeton)KLF8
Genetics Home Reference (NIH)KLF8
Genomic and cartography
GoldenPath hg19 (UCSC)KLF8  -     chrX:56258870-56314322 +  Xp11.21   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)KLF8  -     Xp11.21   [Description]    (hg38-Dec_2013)
EnsemblKLF8 - Xp11.21 [CytoView hg19]  KLF8 - Xp11.21 [CytoView hg38]
Mapping of homologs : NCBIKLF8 [Mapview hg19]  KLF8 [Mapview hg38]
OMIM300286   
Gene and transcription
Genbank (Entrez)AB209004 AK054627 AK296156 BC031355 BC063276
RefSeq transcript (Entrez)NM_001159296 NM_007250
RefSeq genomic (Entrez)NC_000023 NC_018934 NG_011949 NT_011630 NW_004929442
Consensus coding sequences : CCDS (NCBI)KLF8
Cluster EST : UnigeneHs.646614 [ NCBI ]
CGAP (NCI)Hs.646614
Alternative Splicing GalleryENSG00000102349
Gene ExpressionKLF8 [ NCBI-GEO ]   KLF8 [ EBI - ARRAY_EXPRESS ]   KLF8 [ SEEK ]   KLF8 [ MEM ]
Gene Expression Viewer (FireBrowse)KLF8 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)11279
GTEX Portal (Tissue expression)KLF8
Protein : pattern, domain, 3D structure
UniProt/SwissProtO95600   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO95600  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO95600
Splice isoforms : SwissVarO95600
PhosPhoSitePlusO95600
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)KLF8
DMDM Disease mutations11279
Blocks (Seattle)KLF8
SuperfamilyO95600
Human Protein AtlasENSG00000102349
Peptide AtlasO95600
HPRD02238
IPIIPI00478866   IPI00641646   IPI00981600   
Protein Interaction databases
DIP (DOE-UCLA)O95600
IntAct (EBI)O95600
FunCoupENSG00000102349
BioGRIDKLF8
STRING (EMBL)KLF8
ZODIACKLF8
Ontologies - Pathways
QuickGOO95600
Ontology : AmiGODNA binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  metal ion binding  
Ontology : EGO-EBIDNA binding  nucleus  transcription, DNA-templated  regulation of transcription, DNA-templated  metal ion binding  
NDEx NetworkKLF8
Atlas of Cancer Signalling NetworkKLF8
Wikipedia pathwaysKLF8
Orthology - Evolution
OrthoDB11279
GeneTree (enSembl)ENSG00000102349
Phylogenetic Trees/Animal Genes : TreeFamKLF8
HOVERGENO95600
HOGENOMO95600
Homologs : HomoloGeneKLF8
Homology/Alignments : Family Browser (UCSC)KLF8
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKLF8 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KLF8
dbVarKLF8
ClinVarKLF8
1000_GenomesKLF8 
Exome Variant ServerKLF8
ExAC (Exome Aggregation Consortium)KLF8 (select the gene name)
Genetic variants : HAPMAP11279
Genomic Variants (DGV)KLF8 [DGVbeta]
DECIPHER (Syndromes)X:56258870-56314322  ENSG00000102349
CONAN: Copy Number AnalysisKLF8 
Mutations
ICGC Data PortalKLF8 
TCGA Data PortalKLF8 
Broad Tumor PortalKLF8
OASIS PortalKLF8 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKLF8  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDKLF8
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch KLF8
DgiDB (Drug Gene Interaction Database)KLF8
DoCM (Curated mutations)KLF8 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KLF8 (select a term)
intoGenKLF8
Cancer3DKLF8(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM300286   
Orphanet
MedgenKLF8
Genetic Testing Registry KLF8
NextProtO95600 [Medical]
TSGene11279
GENETestsKLF8
Huge Navigator KLF8 [HugePedia]
snp3D : Map Gene to Disease11279
BioCentury BCIQKLF8
ClinGenKLF8 (curated)
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD11279
Chemical/Pharm GKB GenePA30141
Clinical trialKLF8
Miscellaneous
canSAR (ICR)KLF8 (select the gene name)
Probes
Litterature
PubMed43 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKLF8
EVEXKLF8
GoPubMedKLF8
iHOPKLF8
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 : Tue Mar 14 13:12:03 CET 2017

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