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KIAA1522 (KIAA1522)

Identity

Other alias-
HGNC (Hugo) KIAA1522
LocusID (NCBI) 57648
Atlas_Id 64887
Location 1p35.1  [Link to chromosome band 1p35]
Location_base_pair Starts at 32765634 and ends at 32774970 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
BAG6 (6p21.33) / KIAA1522 (1p35.1)SHB (9p13.2) / KIAA1522 (1p35.1)TMEM9 (1q32.1) / KIAA1522 (1p35.1)

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)KIAA1522   29301
Cards
Entrez_Gene (NCBI)KIAA1522  57648  KIAA1522
Aliases
GeneCards (Weizmann)KIAA1522
Ensembl hg19 (Hinxton)ENSG00000162522 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000162522 [Gene_View]  chr1:32765634-32774970 [Contig_View]  KIAA1522 [Vega]
ICGC DataPortalENSG00000162522
TCGA cBioPortalKIAA1522
AceView (NCBI)KIAA1522
Genatlas (Paris)KIAA1522
WikiGenes57648
SOURCE (Princeton)KIAA1522
Genetics Home Reference (NIH)KIAA1522
Genomic and cartography
GoldenPath hg38 (UCSC)KIAA1522  -     chr1:32765634-32774970 +  1p35.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)KIAA1522  -     1p35.1   [Description]    (hg19-Feb_2009)
EnsemblKIAA1522 - 1p35.1 [CytoView hg19]  KIAA1522 - 1p35.1 [CytoView hg38]
Mapping of homologs : NCBIKIAA1522 [Mapview hg19]  KIAA1522 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB040955 AI587184 AK298965 AL713671 AL833933
RefSeq transcript (Entrez)NM_001198972 NM_001198973 NM_020888
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)KIAA1522
Cluster EST : UnigeneHs.591502 [ NCBI ]
CGAP (NCI)Hs.591502
Alternative Splicing GalleryENSG00000162522
Gene ExpressionKIAA1522 [ NCBI-GEO ]   KIAA1522 [ EBI - ARRAY_EXPRESS ]   KIAA1522 [ SEEK ]   KIAA1522 [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA1522 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)57648
GTEX Portal (Tissue expression)KIAA1522
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9P206   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9P206  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9P206
Splice isoforms : SwissVarQ9P206
PhosPhoSitePlusQ9P206
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)KIAA1522
DMDM Disease mutations57648
Blocks (Seattle)KIAA1522
SuperfamilyQ9P206
Human Protein AtlasENSG00000162522
Peptide AtlasQ9P206
IPIIPI00872465   IPI00001632   IPI00936576   IPI00974026   
Protein Interaction databases
DIP (DOE-UCLA)Q9P206
IntAct (EBI)Q9P206
FunCoupENSG00000162522
BioGRIDKIAA1522
STRING (EMBL)KIAA1522
ZODIACKIAA1522
Ontologies - Pathways
QuickGOQ9P206
Ontology : AmiGOcell differentiation  
Ontology : EGO-EBIcell differentiation  
NDEx NetworkKIAA1522
Atlas of Cancer Signalling NetworkKIAA1522
Wikipedia pathwaysKIAA1522
Orthology - Evolution
OrthoDB57648
GeneTree (enSembl)ENSG00000162522
Phylogenetic Trees/Animal Genes : TreeFamKIAA1522
HOVERGENQ9P206
HOGENOMQ9P206
Homologs : HomoloGeneKIAA1522
Homology/Alignments : Family Browser (UCSC)KIAA1522
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA1522 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KIAA1522
dbVarKIAA1522
ClinVarKIAA1522
1000_GenomesKIAA1522 
Exome Variant ServerKIAA1522
ExAC (Exome Aggregation Consortium)KIAA1522 (select the gene name)
Genetic variants : HAPMAP57648
Genomic Variants (DGV)KIAA1522 [DGVbeta]
DECIPHERKIAA1522 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisKIAA1522 
Mutations
ICGC Data PortalKIAA1522 
TCGA Data PortalKIAA1522 
Broad Tumor PortalKIAA1522
OASIS PortalKIAA1522 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKIAA1522  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDKIAA1522
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 KIAA1522
DgiDB (Drug Gene Interaction Database)KIAA1522
DoCM (Curated mutations)KIAA1522 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KIAA1522 (select a term)
intoGenKIAA1522
Cancer3DKIAA1522(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenKIAA1522
Genetic Testing Registry KIAA1522
NextProtQ9P206 [Medical]
TSGene57648
GENETestsKIAA1522
Target ValidationKIAA1522
Huge Navigator KIAA1522 [HugePedia]
snp3D : Map Gene to Disease57648
BioCentury BCIQKIAA1522
ClinGenKIAA1522
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD57648
Chemical/Pharm GKB GenePA142671612
Clinical trialKIAA1522
Miscellaneous
canSAR (ICR)KIAA1522 (select the gene name)
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKIAA1522
EVEXKIAA1522
GoPubMedKIAA1522
iHOPKIAA1522
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 13:11:51 CEST 2017

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