Atlas of Genetics and Cytogenetics in Oncology and Haematology


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KLHL34 (kelch-like family member 34)

Identity

Alias_nameskelch-like 34 (Drosophila)
Alias_symbol (synonym)FLJ34960
RP11-450P7.3
Other alias-
HGNC (Hugo) KLHL34
LocusID (NCBI) 257240
Atlas_Id 64977
Location Xp22.12  [Link to chromosome band Xp22]
Location_base_pair Starts at 21673467 and ends at 21676505 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)KLHL34   26634
Cards
Entrez_Gene (NCBI)KLHL34  257240  kelch-like family member 34
Aliases
GeneCards (Weizmann)KLHL34
Ensembl hg19 (Hinxton)ENSG00000185915 [Gene_View]  chrX:21673467-21676505 [Contig_View]  KLHL34 [Vega]
Ensembl hg38 (Hinxton)ENSG00000185915 [Gene_View]  chrX:21673467-21676505 [Contig_View]  KLHL34 [Vega]
ICGC DataPortalENSG00000185915
TCGA cBioPortalKLHL34
AceView (NCBI)KLHL34
Genatlas (Paris)KLHL34
WikiGenes257240
SOURCE (Princeton)KLHL34
Genetics Home Reference (NIH)KLHL34
Genomic and cartography
GoldenPath hg19 (UCSC)KLHL34  -     chrX:21673467-21676505 -  Xp22.12   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)KLHL34  -     Xp22.12   [Description]    (hg38-Dec_2013)
EnsemblKLHL34 - Xp22.12 [CytoView hg19]  KLHL34 - Xp22.12 [CytoView hg38]
Mapping of homologs : NCBIKLHL34 [Mapview hg19]  KLHL34 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI792176 AK092279 BC109031 DA395149
RefSeq transcript (Entrez)NM_153270
RefSeq genomic (Entrez)NC_000023 NC_018934 NT_167197 NW_004929438
Consensus coding sequences : CCDS (NCBI)KLHL34
Cluster EST : UnigeneHs.448572 [ NCBI ]
CGAP (NCI)Hs.448572
Alternative Splicing GalleryENSG00000185915
Gene ExpressionKLHL34 [ NCBI-GEO ]   KLHL34 [ EBI - ARRAY_EXPRESS ]   KLHL34 [ SEEK ]   KLHL34 [ MEM ]
Gene Expression Viewer (FireBrowse)KLHL34 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)257240
GTEX Portal (Tissue expression)KLHL34
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N239   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N239  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N239
Splice isoforms : SwissVarQ8N239
PhosPhoSitePlusQ8N239
Domaine pattern : Prosite (Expaxy)BTB (PS50097)   
Domains : Interpro (EBI)BACK    BTB-kelch_protein    BTB/POZ-like    BTB/POZ_fold    BTB_POZ    Kelch-typ_b-propeller    Kelch_1   
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)KLHL34
DMDM Disease mutations257240
Blocks (Seattle)KLHL34
SuperfamilyQ8N239
Human Protein AtlasENSG00000185915
Peptide AtlasQ8N239
HPRD06558
IPIIPI00166264   
Protein Interaction databases
DIP (DOE-UCLA)Q8N239
IntAct (EBI)Q8N239
FunCoupENSG00000185915
BioGRIDKLHL34
STRING (EMBL)KLHL34
ZODIACKLHL34
Ontologies - Pathways
QuickGOQ8N239
Ontology : AmiGOextracellular space  
Ontology : EGO-EBIextracellular space  
NDEx NetworkKLHL34
Atlas of Cancer Signalling NetworkKLHL34
Wikipedia pathwaysKLHL34
Orthology - Evolution
OrthoDB257240
GeneTree (enSembl)ENSG00000185915
Phylogenetic Trees/Animal Genes : TreeFamKLHL34
HOVERGENQ8N239
HOGENOMQ8N239
Homologs : HomoloGeneKLHL34
Homology/Alignments : Family Browser (UCSC)KLHL34
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKLHL34 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KLHL34
dbVarKLHL34
ClinVarKLHL34
1000_GenomesKLHL34 
Exome Variant ServerKLHL34
ExAC (Exome Aggregation Consortium)KLHL34 (select the gene name)
Genetic variants : HAPMAP257240
Genomic Variants (DGV)KLHL34 [DGVbeta]
DECIPHER (Syndromes)X:21673467-21676505  ENSG00000185915
CONAN: Copy Number AnalysisKLHL34 
Mutations
ICGC Data PortalKLHL34 
TCGA Data PortalKLHL34 
Broad Tumor PortalKLHL34
OASIS PortalKLHL34 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKLHL34  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDKLHL34
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch KLHL34
DgiDB (Drug Gene Interaction Database)KLHL34
DoCM (Curated mutations)KLHL34 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KLHL34 (select a term)
intoGenKLHL34
Cancer3DKLHL34(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenKLHL34
Genetic Testing Registry KLHL34
NextProtQ8N239 [Medical]
TSGene257240
GENETestsKLHL34
Huge Navigator KLHL34 [HugePedia]
snp3D : Map Gene to Disease257240
BioCentury BCIQKLHL34
ClinGenKLHL34
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD257240
Chemical/Pharm GKB GenePA162393594
Clinical trialKLHL34
Miscellaneous
canSAR (ICR)KLHL34 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKLHL34
EVEXKLHL34
GoPubMedKLHL34
iHOPKLHL34
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 12:10:03 CET 2017

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