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KIAA1586 (KIAA1586)

Identity

Other alias-
HGNC (Hugo) KIAA1586
LocusID (NCBI) 57691
Atlas_Id 64890
Location 6p12.1  [Link to chromosome band 6p12]
Location_base_pair Starts at 57046532 and ends at 57055239 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)

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)KIAA1586   21360
Cards
Entrez_Gene (NCBI)KIAA1586  57691  KIAA1586
Aliases
GeneCards (Weizmann)KIAA1586
Ensembl hg19 (Hinxton)ENSG00000168116 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000168116 [Gene_View]  ENSG00000168116 [Sequence]  chr6:57046532-57055239 [Contig_View]  KIAA1586 [Vega]
ICGC DataPortalENSG00000168116
TCGA cBioPortalKIAA1586
AceView (NCBI)KIAA1586
Genatlas (Paris)KIAA1586
WikiGenes57691
SOURCE (Princeton)KIAA1586
Genetics Home Reference (NIH)KIAA1586
Genomic and cartography
GoldenPath hg38 (UCSC)KIAA1586  -     chr6:57046532-57055239 +  6p12.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)KIAA1586  -     6p12.1   [Description]    (hg19-Feb_2009)
EnsemblKIAA1586 - 6p12.1 [CytoView hg19]  KIAA1586 - 6p12.1 [CytoView hg38]
Mapping of homologs : NCBIKIAA1586 [Mapview hg19]  KIAA1586 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB046806 AK290988 AK295519 BC012011 BC029372
RefSeq transcript (Entrez)NM_001286274 NM_001286275 NM_001286276 NM_020931
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)KIAA1586
Cluster EST : UnigeneHs.709521 [ NCBI ]
CGAP (NCI)Hs.709521
Alternative Splicing GalleryENSG00000168116
Gene ExpressionKIAA1586 [ NCBI-GEO ]   KIAA1586 [ EBI - ARRAY_EXPRESS ]   KIAA1586 [ SEEK ]   KIAA1586 [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA1586 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)57691
GTEX Portal (Tissue expression)KIAA1586
Human Protein AtlasENSG00000168116-KIAA1586 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9HCI6   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9HCI6  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9HCI6
Splice isoforms : SwissVarQ9HCI6
PhosPhoSitePlusQ9HCI6
Domains : Interpro (EBI)RNaseH-like_dom   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)KIAA1586
DMDM Disease mutations57691
Blocks (Seattle)KIAA1586
SuperfamilyQ9HCI6
Human Protein Atlas [tissue]ENSG00000168116-KIAA1586 [tissue]
Peptide AtlasQ9HCI6
HPRD17218
IPIIPI00259113   IPI00885066   
Protein Interaction databases
DIP (DOE-UCLA)Q9HCI6
IntAct (EBI)Q9HCI6
FunCoupENSG00000168116
BioGRIDKIAA1586
STRING (EMBL)KIAA1586
ZODIACKIAA1586
Ontologies - Pathways
QuickGOQ9HCI6
Ontology : AmiGOnucleic acid binding  ligase activity  protein sumoylation  protein sumoylation  SUMO ligase activity  
Ontology : EGO-EBInucleic acid binding  ligase activity  protein sumoylation  protein sumoylation  SUMO ligase activity  
NDEx NetworkKIAA1586
Atlas of Cancer Signalling NetworkKIAA1586
Wikipedia pathwaysKIAA1586
Orthology - Evolution
OrthoDB57691
GeneTree (enSembl)ENSG00000168116
Phylogenetic Trees/Animal Genes : TreeFamKIAA1586
HOVERGENQ9HCI6
HOGENOMQ9HCI6
Homologs : HomoloGeneKIAA1586
Homology/Alignments : Family Browser (UCSC)KIAA1586
Gene fusions - Rearrangements
Fusion : QuiverKIAA1586
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA1586 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KIAA1586
dbVarKIAA1586
ClinVarKIAA1586
1000_GenomesKIAA1586 
Exome Variant ServerKIAA1586
ExAC (Exome Aggregation Consortium)ENSG00000168116
GNOMAD BrowserENSG00000168116
Varsome BrowserKIAA1586
Genetic variants : HAPMAP57691
Genomic Variants (DGV)KIAA1586 [DGVbeta]
DECIPHERKIAA1586 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisKIAA1586 
Mutations
ICGC Data PortalKIAA1586 
TCGA Data PortalKIAA1586 
Broad Tumor PortalKIAA1586
OASIS PortalKIAA1586 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKIAA1586  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDKIAA1586
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 KIAA1586
DgiDB (Drug Gene Interaction Database)KIAA1586
DoCM (Curated mutations)KIAA1586 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KIAA1586 (select a term)
intoGenKIAA1586
Cancer3DKIAA1586(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETKIAA1586
MedgenKIAA1586
Genetic Testing Registry KIAA1586
NextProtQ9HCI6 [Medical]
TSGene57691
GENETestsKIAA1586
Target ValidationKIAA1586
Huge Navigator KIAA1586 [HugePedia]
snp3D : Map Gene to Disease57691
BioCentury BCIQKIAA1586
ClinGenKIAA1586
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD57691
Chemical/Pharm GKB GenePA134963244
Clinical trialKIAA1586
Miscellaneous
canSAR (ICR)KIAA1586 (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKIAA1586
EVEXKIAA1586
GoPubMedKIAA1586
iHOPKIAA1586
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Jul 30 13:50:56 CEST 2018

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