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AHSA2 (activator of HSP90 ATPase homolog 2)

Identity

Alias_symbol (synonym)DKFZp564C236
Hch1
Other aliasAHA1
HGNC (Hugo) AHSA2
LocusID (NCBI) 130872
Atlas_Id 47361
Location 2p15  [Link to chromosome band 2p15]
Location_base_pair Starts at 61177418 and ends at 61187551 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
BCAM (19q13.32) / AHSA2 (2p15)

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)AHSA2   20437
Cards
Entrez_Gene (NCBI)AHSA2  130872  activator of HSP90 ATPase homolog 2
AliasesAHA1; Hch1
GeneCards (Weizmann)AHSA2
Ensembl hg19 (Hinxton)ENSG00000173209 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000173209 [Gene_View]  chr2:61177418-61187551 [Contig_View]  AHSA2 [Vega]
ICGC DataPortalENSG00000173209
TCGA cBioPortalAHSA2
AceView (NCBI)AHSA2
Genatlas (Paris)AHSA2
WikiGenes130872
SOURCE (Princeton)AHSA2
Genetics Home Reference (NIH)AHSA2
Genomic and cartography
GoldenPath hg38 (UCSC)AHSA2  -     chr2:61177418-61187551 +  2p15   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)AHSA2  -     2p15   [Description]    (hg19-Feb_2009)
EnsemblAHSA2 - 2p15 [CytoView hg19]  AHSA2 - 2p15 [CytoView hg38]
Mapping of homologs : NCBIAHSA2 [Mapview hg19]  AHSA2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA856729 AF542548 AI636364 AK091998 AK092505
RefSeq transcript (Entrez)NM_001321300 NM_001321301 NM_001321302 NM_001321303 NM_001321304 NM_001321305 NM_152392
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)AHSA2
Cluster EST : UnigeneHs.732993 [ NCBI ]
CGAP (NCI)Hs.732993
Alternative Splicing GalleryENSG00000173209
Gene ExpressionAHSA2 [ NCBI-GEO ]   AHSA2 [ EBI - ARRAY_EXPRESS ]   AHSA2 [ SEEK ]   AHSA2 [ MEM ]
Gene Expression Viewer (FireBrowse)AHSA2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)130872
GTEX Portal (Tissue expression)AHSA2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ719I0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ719I0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ719I0
Splice isoforms : SwissVarQ719I0
PhosPhoSitePlusQ719I0
Domains : Interpro (EBI)AHSA1_N   
Domain families : Pfam (Sanger)Aha1_N (PF09229)   
Domain families : Pfam (NCBI)pfam09229   
Domain families : Smart (EMBL)Aha1_N (SM01000)  
Conserved Domain (NCBI)AHSA2
DMDM Disease mutations130872
Blocks (Seattle)AHSA2
SuperfamilyQ719I0
Human Protein AtlasENSG00000173209
Peptide AtlasQ719I0
HPRD16479
IPIIPI00168592   IPI00873311   IPI00783340   IPI00942660   IPI00917133   
Protein Interaction databases
DIP (DOE-UCLA)Q719I0
IntAct (EBI)Q719I0
FunCoupENSG00000173209
BioGRIDAHSA2
STRING (EMBL)AHSA2
ZODIACAHSA2
Ontologies - Pathways
QuickGOQ719I0
Ontology : AmiGOATPase activator activity  protein binding  positive regulation of ATPase activity  chaperone binding  
Ontology : EGO-EBIATPase activator activity  protein binding  positive regulation of ATPase activity  chaperone binding  
NDEx NetworkAHSA2
Atlas of Cancer Signalling NetworkAHSA2
Wikipedia pathwaysAHSA2
Orthology - Evolution
OrthoDB130872
GeneTree (enSembl)ENSG00000173209
Phylogenetic Trees/Animal Genes : TreeFamAHSA2
HOVERGENQ719I0
HOGENOMQ719I0
Homologs : HomoloGeneAHSA2
Homology/Alignments : Family Browser (UCSC)AHSA2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerAHSA2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)AHSA2
dbVarAHSA2
ClinVarAHSA2
1000_GenomesAHSA2 
Exome Variant ServerAHSA2
ExAC (Exome Aggregation Consortium)AHSA2 (select the gene name)
Genetic variants : HAPMAP130872
Genomic Variants (DGV)AHSA2 [DGVbeta]
DECIPHERAHSA2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisAHSA2 
Mutations
ICGC Data PortalAHSA2 
TCGA Data PortalAHSA2 
Broad Tumor PortalAHSA2
OASIS PortalAHSA2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICAHSA2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDAHSA2
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 AHSA2
DgiDB (Drug Gene Interaction Database)AHSA2
DoCM (Curated mutations)AHSA2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)AHSA2 (select a term)
intoGenAHSA2
Cancer3DAHSA2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenAHSA2
Genetic Testing Registry AHSA2
NextProtQ719I0 [Medical]
TSGene130872
GENETestsAHSA2
Target ValidationAHSA2
Huge Navigator AHSA2 [HugePedia]
snp3D : Map Gene to Disease130872
BioCentury BCIQAHSA2
ClinGenAHSA2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD130872
Chemical/Pharm GKB GenePA134913389
Clinical trialAHSA2
Miscellaneous
canSAR (ICR)AHSA2 (select the gene name)
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineAHSA2
EVEXAHSA2
GoPubMedAHSA2
iHOPAHSA2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed Jun 7 12:23:13 CEST 2017

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