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KLHL14 (kelch-like family member 14)

Identity

Alias_nameskelch-like 14 (Drosophila)
Alias_symbol (synonym)KIAA1384
Other alias-
HGNC (Hugo) KLHL14
LocusID (NCBI) 57565
Atlas_Id 64962
Location 18q12.1  [Link to chromosome band 18q12]
Location_base_pair Starts at 30252634 and ends at 30352974 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)KLHL14   29266
Cards
Entrez_Gene (NCBI)KLHL14  57565  kelch-like family member 14
Aliases
GeneCards (Weizmann)KLHL14
Ensembl hg19 (Hinxton)ENSG00000197705 [Gene_View]  chr18:30252634-30352974 [Contig_View]  KLHL14 [Vega]
Ensembl hg38 (Hinxton)ENSG00000197705 [Gene_View]  chr18:30252634-30352974 [Contig_View]  KLHL14 [Vega]
ICGC DataPortalENSG00000197705
TCGA cBioPortalKLHL14
AceView (NCBI)KLHL14
Genatlas (Paris)KLHL14
WikiGenes57565
SOURCE (Princeton)KLHL14
Genetics Home Reference (NIH)KLHL14
Genomic and cartography
GoldenPath hg19 (UCSC)KLHL14  -     chr18:30252634-30352974 -  18q12.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)KLHL14  -     18q12.1   [Description]    (hg38-Dec_2013)
EnsemblKLHL14 - 18q12.1 [CytoView hg19]  KLHL14 - 18q12.1 [CytoView hg38]
Mapping of homologs : NCBIKLHL14 [Mapview hg19]  KLHL14 [Mapview hg38]
OMIM613772   
Gene and transcription
Genbank (Entrez)AB037805 AK294996 BC021267
RefSeq transcript (Entrez)NM_020805
RefSeq genomic (Entrez)NC_000018 NC_018929 NT_010966 NW_004929410
Consensus coding sequences : CCDS (NCBI)KLHL14
Cluster EST : UnigeneHs.446164 [ NCBI ]
CGAP (NCI)Hs.446164
Alternative Splicing GalleryENSG00000197705
Gene ExpressionKLHL14 [ NCBI-GEO ]   KLHL14 [ EBI - ARRAY_EXPRESS ]   KLHL14 [ SEEK ]   KLHL14 [ MEM ]
Gene Expression Viewer (FireBrowse)KLHL14 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)57565
GTEX Portal (Tissue expression)KLHL14
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9P2G3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9P2G3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9P2G3
Splice isoforms : SwissVarQ9P2G3
PhosPhoSitePlusQ9P2G3
Domaine pattern : Prosite (Expaxy)BTB (PS50097)   
Domains : Interpro (EBI)BACK    BTB/POZ-like    BTB/POZ_fold    BTB_POZ    Kelch-typ_b-propeller    Kelch_1    KLHL14   
Domain families : Pfam (Sanger)BACK (PF07707)    BTB (PF00651)    Kelch_1 (PF01344)   
Domain families : Pfam (NCBI)pfam07707    pfam00651    pfam01344   
Domain families : Smart (EMBL)BACK (SM00875)  BTB (SM00225)  Kelch (SM00612)  
Conserved Domain (NCBI)KLHL14
DMDM Disease mutations57565
Blocks (Seattle)KLHL14
SuperfamilyQ9P2G3
Human Protein AtlasENSG00000197705
Peptide AtlasQ9P2G3
HPRD17238
IPIIPI00783144   IPI00418195   
Protein Interaction databases
DIP (DOE-UCLA)Q9P2G3
IntAct (EBI)Q9P2G3
FunCoupENSG00000197705
BioGRIDKLHL14
STRING (EMBL)KLHL14
ZODIACKLHL14
Ontologies - Pathways
QuickGOQ9P2G3
Ontology : AmiGOendoplasmic reticulum  endoplasmic reticulum membrane  cytosol  neuron projection  neuronal cell body  
Ontology : EGO-EBIendoplasmic reticulum  endoplasmic reticulum membrane  cytosol  neuron projection  neuronal cell body  
NDEx NetworkKLHL14
Atlas of Cancer Signalling NetworkKLHL14
Wikipedia pathwaysKLHL14
Orthology - Evolution
OrthoDB57565
GeneTree (enSembl)ENSG00000197705
Phylogenetic Trees/Animal Genes : TreeFamKLHL14
HOVERGENQ9P2G3
HOGENOMQ9P2G3
Homologs : HomoloGeneKLHL14
Homology/Alignments : Family Browser (UCSC)KLHL14
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKLHL14 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KLHL14
dbVarKLHL14
ClinVarKLHL14
1000_GenomesKLHL14 
Exome Variant ServerKLHL14
ExAC (Exome Aggregation Consortium)KLHL14 (select the gene name)
Genetic variants : HAPMAP57565
Genomic Variants (DGV)KLHL14 [DGVbeta]
DECIPHER (Syndromes)18:30252634-30352974  ENSG00000197705
CONAN: Copy Number AnalysisKLHL14 
Mutations
ICGC Data PortalKLHL14 
TCGA Data PortalKLHL14 
Broad Tumor PortalKLHL14
OASIS PortalKLHL14 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKLHL14  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDKLHL14
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 KLHL14
DgiDB (Drug Gene Interaction Database)KLHL14
DoCM (Curated mutations)KLHL14 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KLHL14 (select a term)
intoGenKLHL14
Cancer3DKLHL14(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM613772   
Orphanet
MedgenKLHL14
Genetic Testing Registry KLHL14
NextProtQ9P2G3 [Medical]
TSGene57565
GENETestsKLHL14
Huge Navigator KLHL14 [HugePedia]
snp3D : Map Gene to Disease57565
BioCentury BCIQKLHL14
ClinGenKLHL14
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD57565
Chemical/Pharm GKB GenePA134945930
Clinical trialKLHL14
Miscellaneous
canSAR (ICR)KLHL14 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKLHL14
EVEXKLHL14
GoPubMedKLHL14
iHOPKLHL14
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Mar 14 12:10:00 CET 2017

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