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KLHDC10 (kelch domain containing 10)

Identity

Alias (NCBI)slim
HGNC (Hugo) KLHDC10
HGNC Alias symbKIAA0265
slim
HGNC Alias namescruin like at the midline homolog (Drosophila)
LocusID (NCBI) 23008
Atlas_Id 64953
Location 7q32.2  [Link to chromosome band 7q32]
Location_base_pair Starts at 130070534 and ends at 130135705 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
ELP4 (11p13) / KLHDC10 (7q32.2)

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)KLHDC10   22194
Cards
Entrez_Gene (NCBI)KLHDC10    kelch domain containing 10
Aliasesslim
GeneCards (Weizmann)KLHDC10
Ensembl hg19 (Hinxton)ENSG00000128607 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000128607 [Gene_View]  ENSG00000128607 [Sequence]  chr7:130070534-130135705 [Contig_View]  KLHDC10 [Vega]
ICGC DataPortalENSG00000128607
TCGA cBioPortalKLHDC10
AceView (NCBI)KLHDC10
Genatlas (Paris)KLHDC10
SOURCE (Princeton)KLHDC10
Genetics Home Reference (NIH)KLHDC10
Genomic and cartography
GoldenPath hg38 (UCSC)KLHDC10  -     chr7:130070534-130135705 +  7q32.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)KLHDC10  -     7q32.2   [Description]    (hg19-Feb_2009)
GoldenPathKLHDC10 - 7q32.2 [CytoView hg19]  KLHDC10 - 7q32.2 [CytoView hg38]
ImmunoBaseENSG00000128607
Genome Data Viewer NCBIKLHDC10 [Mapview hg19]  
OMIM615152   
Gene and transcription
Genbank (Entrez)AF277177 BC009977 BC036464 BC044884 D87454
RefSeq transcript (Entrez)NM_014997
Consensus coding sequences : CCDS (NCBI)KLHDC10
Gene ExpressionKLHDC10 [ NCBI-GEO ]   KLHDC10 [ EBI - ARRAY_EXPRESS ]   KLHDC10 [ SEEK ]   KLHDC10 [ MEM ]
Gene Expression Viewer (FireBrowse)KLHDC10 [ Firebrowse - Broad ]
GenevisibleExpression of KLHDC10 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)23008
GTEX Portal (Tissue expression)KLHDC10
Human Protein AtlasENSG00000128607-KLHDC10 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6PID8   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6PID8  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6PID8
PhosPhoSitePlusQ6PID8
Domains : Interpro (EBI)Kelch-typ_b-propeller    Kelch_1   
Domain families : Pfam (Sanger)Kelch_1 (PF01344)   
Domain families : Pfam (NCBI)pfam01344   
Domain families : Smart (EMBL)Kelch (SM00612)  
Conserved Domain (NCBI)KLHDC10
SuperfamilyQ6PID8
AlphaFold pdb e-kbQ6PID8   
Human Protein Atlas [tissue]ENSG00000128607-KLHDC10 [tissue]
HPRD17182
Protein Interaction databases
DIP (DOE-UCLA)Q6PID8
IntAct (EBI)Q6PID8
BioGRIDKLHDC10
STRING (EMBL)KLHDC10
ZODIACKLHDC10
Ontologies - Pathways
QuickGOQ6PID8
Ontology : AmiGOprotein binding  nucleoplasm  cytoplasm  positive regulation of stress-activated MAPK cascade  
Ontology : EGO-EBIprotein binding  nucleoplasm  cytoplasm  positive regulation of stress-activated MAPK cascade  
NDEx NetworkKLHDC10
Atlas of Cancer Signalling NetworkKLHDC10
Wikipedia pathwaysKLHDC10
Orthology - Evolution
OrthoDB23008
GeneTree (enSembl)ENSG00000128607
Phylogenetic Trees/Animal Genes : TreeFamKLHDC10
Homologs : HomoloGeneKLHDC10
Homology/Alignments : Family Browser (UCSC)KLHDC10
Gene fusions - Rearrangements
Fusion : QuiverKLHDC10
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKLHDC10 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KLHDC10
dbVarKLHDC10
ClinVarKLHDC10
MonarchKLHDC10
1000_GenomesKLHDC10 
Exome Variant ServerKLHDC10
GNOMAD BrowserENSG00000128607
Varsome BrowserKLHDC10
ACMGKLHDC10 variants
VarityQ6PID8
Genomic Variants (DGV)KLHDC10 [DGVbeta]
DECIPHERKLHDC10 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisKLHDC10 
Mutations
ICGC Data PortalKLHDC10 
TCGA Data PortalKLHDC10 
Broad Tumor PortalKLHDC10
OASIS PortalKLHDC10 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKLHDC10  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DKLHDC10
Mutations and Diseases : HGMDKLHDC10
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaKLHDC10
DgiDB (Drug Gene Interaction Database)KLHDC10
DoCM (Curated mutations)KLHDC10
CIViC (Clinical Interpretations of Variants in Cancer)KLHDC10
Cancer3DKLHDC10
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM615152   
Orphanet
DisGeNETKLHDC10
MedgenKLHDC10
Genetic Testing Registry KLHDC10
NextProtQ6PID8 [Medical]
GENETestsKLHDC10
Target ValidationKLHDC10
Huge Navigator KLHDC10 [HugePedia]
ClinGenKLHDC10
Clinical trials, drugs, therapy
MyCancerGenomeKLHDC10
Protein Interactions : CTDKLHDC10
Pharm GKB GenePA164721976
PharosQ6PID8
Clinical trialKLHDC10
Miscellaneous
canSAR (ICR)KLHDC10
HarmonizomeKLHDC10
DataMed IndexKLHDC10
Probes
Litterature
PubMed23 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXKLHDC10
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:54:43 CEST 2021

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