Atlas of Genetics and Cytogenetics in Oncology and Haematology


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KIAA2026 (KIAA2026)

Identity

Alias_symbol (synonym)FLJ20375
Other alias-
HGNC (Hugo) KIAA2026
LocusID (NCBI) 158358
Atlas_Id 64909
Location 9p24.1  [Link to chromosome band 9p24]
Location_base_pair Starts at 5919008 and ends at 6008003 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
BGN (Xq28) / KIAA2026 (9p24.1)KIAA2026 (9p24.1) / C2orf74 (2p15)KIAA2026 (9p24.1) / CALD1 (7q33)
KIAA2026 (9p24.1) / CMTM7 (3p22.3)KIAA2026 (9p24.1) / KIAA2026 (9p24.1)KIAA2026 (9p24.1) / MMACHC (1p34.1)
KIAA2026 (9p24.1) / PAPPA (9q33.1)KIAA2026 (9p24.1) / TMEM232 (5q22.1)

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)KIAA2026   23378
Cards
Entrez_Gene (NCBI)KIAA2026  158358  KIAA2026
Aliases
GeneCards (Weizmann)KIAA2026
Ensembl hg19 (Hinxton)ENSG00000183354 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000183354 [Gene_View]  chr9:5919008-6008003 [Contig_View]  KIAA2026 [Vega]
ICGC DataPortalENSG00000183354
TCGA cBioPortalKIAA2026
AceView (NCBI)KIAA2026
Genatlas (Paris)KIAA2026
WikiGenes158358
SOURCE (Princeton)KIAA2026
Genetics Home Reference (NIH)KIAA2026
Genomic and cartography
GoldenPath hg38 (UCSC)KIAA2026  -     chr9:5919008-6008003 -  9p24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)KIAA2026  -     9p24.1   [Description]    (hg19-Feb_2009)
EnsemblKIAA2026 - 9p24.1 [CytoView hg19]  KIAA2026 - 9p24.1 [CytoView hg38]
Mapping of homologs : NCBIKIAA2026 [Mapview hg19]  KIAA2026 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB095946 AL833370 BC136846 BX648372 DY655479
RefSeq transcript (Entrez)NM_001017969
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)KIAA2026
Cluster EST : UnigeneHs.535060 [ NCBI ]
CGAP (NCI)Hs.535060
Alternative Splicing GalleryENSG00000183354
Gene ExpressionKIAA2026 [ NCBI-GEO ]   KIAA2026 [ EBI - ARRAY_EXPRESS ]   KIAA2026 [ SEEK ]   KIAA2026 [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA2026 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)158358
GTEX Portal (Tissue expression)KIAA2026
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5HYC2   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5HYC2  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5HYC2
Splice isoforms : SwissVarQ5HYC2
PhosPhoSitePlusQ5HYC2
Domains : Interpro (EBI)Bromodomain   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)KIAA2026
DMDM Disease mutations158358
Blocks (Seattle)KIAA2026
SuperfamilyQ5HYC2
Human Protein AtlasENSG00000183354
Peptide AtlasQ5HYC2
HPRD18566
IPIIPI00216990   IPI00966688   IPI01012066   IPI01013540   IPI01010815   
Protein Interaction databases
DIP (DOE-UCLA)Q5HYC2
IntAct (EBI)Q5HYC2
FunCoupENSG00000183354
BioGRIDKIAA2026
STRING (EMBL)KIAA2026
ZODIACKIAA2026
Ontologies - Pathways
QuickGOQ5HYC2
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkKIAA2026
Atlas of Cancer Signalling NetworkKIAA2026
Wikipedia pathwaysKIAA2026
Orthology - Evolution
OrthoDB158358
GeneTree (enSembl)ENSG00000183354
Phylogenetic Trees/Animal Genes : TreeFamKIAA2026
HOVERGENQ5HYC2
HOGENOMQ5HYC2
Homologs : HomoloGeneKIAA2026
Homology/Alignments : Family Browser (UCSC)KIAA2026
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA2026 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KIAA2026
dbVarKIAA2026
ClinVarKIAA2026
1000_GenomesKIAA2026 
Exome Variant ServerKIAA2026
ExAC (Exome Aggregation Consortium)KIAA2026 (select the gene name)
Genetic variants : HAPMAP158358
Genomic Variants (DGV)KIAA2026 [DGVbeta]
DECIPHERKIAA2026 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisKIAA2026 
Mutations
ICGC Data PortalKIAA2026 
TCGA Data PortalKIAA2026 
Broad Tumor PortalKIAA2026
OASIS PortalKIAA2026 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKIAA2026  [overview]  [genome browser]  [tissue]  [di{tribqtIon]  
Mutations and Diseases : HGMDKIAA2026
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 KIAA2026
DgiDB (Drug Gene Interaction Database)KIAA2026
DoCM (Curated mutations)KIAA2026 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KIAA2026 (select a term)
intoGenKIAA2026
Cancer3DKIAA2026(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenKIAA2026
Genetic Testing Registry KIAA2026
NextProtQ5HYC2 [Medical]
TSGene158358
GENETestsKIAA2026
Target ValidationKIAA2026
Huge Navigator KIAA2026 [HugePedia]
snp3D : Map Gene to Disease158358
BioCentury BCIQKIAA2026
ClinGenKIAA2026
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD158358
Chemical/Pharm GKB GenePA134907262
Clinical trialKIAA2026
Miscellaneous
canSAR (ICR)KIAA2026 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKIAA2026
EVEXKIAA2026
GoPubMedKIAA2026
iHOPKIAA2026
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:11:54 CEST 2017

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