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KIAA2026 (KIAA2026)

Identity

Alias (NCBI)-
HGNC (Hugo) KIAA2026
HGNC Alias symbFLJ20375
LocusID (NCBI) 158358
Atlas_Id 64909
Location 9p24.1  [Link to chromosome band 9p24]
Location_base_pair Starts at 5919022 and ends at 6008482 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)
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    KIAA2026
Aliases
GeneCards (Weizmann)KIAA2026
Ensembl hg19 (Hinxton)ENSG00000183354 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000183354 [Gene_View]  ENSG00000183354 [Sequence]  chr9:5919022-6008482 [Contig_View]  KIAA2026 [Vega]
ICGC DataPortalENSG00000183354
TCGA cBioPortalKIAA2026
AceView (NCBI)KIAA2026
Genatlas (Paris)KIAA2026
SOURCE (Princeton)KIAA2026
Genetics Home Reference (NIH)KIAA2026
Genomic and cartography
GoldenPath hg38 (UCSC)KIAA2026  -     chr9:5919022-6008482 -  9p24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)KIAA2026  -     9p24.1   [Description]    (hg19-Feb_2009)
GoldenPathKIAA2026 - 9p24.1 [CytoView hg19]  KIAA2026 - 9p24.1 [CytoView hg38]
ImmunoBaseENSG00000183354
Genome Data Viewer NCBIKIAA2026 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AB095946 AL833370 BC136846 BX648372 DY655479
RefSeq transcript (Entrez)NM_001017969
Consensus coding sequences : CCDS (NCBI)KIAA2026
Gene ExpressionKIAA2026 [ NCBI-GEO ]   KIAA2026 [ EBI - ARRAY_EXPRESS ]   KIAA2026 [ SEEK ]   KIAA2026 [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA2026 [ Firebrowse - Broad ]
GenevisibleExpression of KIAA2026 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)158358
GTEX Portal (Tissue expression)KIAA2026
Human Protein AtlasENSG00000183354-KIAA2026 [pathology]   [cell]   [tissue]
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
PhosPhoSitePlusQ5HYC2
Domains : Interpro (EBI)Bromodomain-like_sf    KIAA2026   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)KIAA2026
SuperfamilyQ5HYC2
AlphaFold pdb e-kbQ5HYC2   
Human Protein Atlas [tissue]ENSG00000183354-KIAA2026 [tissue]
HPRD18566
Protein Interaction databases
DIP (DOE-UCLA)Q5HYC2
IntAct (EBI)Q5HYC2
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
Homologs : HomoloGeneKIAA2026
Homology/Alignments : Family Browser (UCSC)KIAA2026
Gene fusions - Rearrangements
Fusion : QuiverKIAA2026
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA2026 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KIAA2026
dbVarKIAA2026
ClinVarKIAA2026
MonarchKIAA2026
1000_GenomesKIAA2026 
Exome Variant ServerKIAA2026
GNOMAD BrowserENSG00000183354
Varsome BrowserKIAA2026
ACMGKIAA2026 variants
VarityQ5HYC2
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]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DKIAA2026
Mutations and Diseases : HGMDKIAA2026
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaKIAA2026
DgiDB (Drug Gene Interaction Database)KIAA2026
DoCM (Curated mutations)KIAA2026
CIViC (Clinical Interpretations of Variants in Cancer)KIAA2026
Cancer3DKIAA2026
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETKIAA2026
MedgenKIAA2026
Genetic Testing Registry KIAA2026
NextProtQ5HYC2 [Medical]
GENETestsKIAA2026
Target ValidationKIAA2026
Huge Navigator KIAA2026 [HugePedia]
ClinGenKIAA2026
Clinical trials, drugs, therapy
MyCancerGenomeKIAA2026
Protein Interactions : CTDKIAA2026
Pharm GKB GenePA134907262
PharosQ5HYC2
Clinical trialKIAA2026
Miscellaneous
canSAR (ICR)KIAA2026
HarmonizomeKIAA2026
DataMed IndexKIAA2026
Probes
Litterature
PubMed11 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXKIAA2026
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 15:54:36 CEST 2021

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