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NAT9 (N-acetyltransferase 9 (putative))

Identity

Alias_namesN-acetyltransferase 9
N-acetyltransferase 9 (GCN5-related, putative)
Alias_symbol (synonym)DKFZP564C103
Other aliasEBSP, hNATL
HGNC (Hugo) NAT9
LocusID (NCBI) 26151
Atlas_Id 70702
Location 17q25.1  [Link to chromosome band 17q25]
Location_base_pair Starts at 74770529 and ends at 74776425 bp from pter ( according to hg38-Dec_2013)

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)NAT9   23133
Cards
Entrez_Gene (NCBI)NAT9  26151  N-acetyltransferase 9 (putative)
AliasesEBSP,
GeneCards (Weizmann)NAT9
Ensembl hg19 (Hinxton)ENSG00000109065 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000109065 [Gene_View]  chr17:74770529-74776425 [Contig_View]  NAT9 [Vega]
ICGC DataPortalENSG00000109065
TCGA cBioPortalNAT9
AceView (NCBI)NAT9
Genatlas (Paris)NAT9
WikiGenes26151
SOURCE (Princeton)NAT9
Genetics Home Reference (NIH)NAT9
Genomic and cartography
GoldenPath hg38 (UCSC)NAT9  -     chr17:74770529-74776425 -  17q25.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)NAT9  -     17q25.1   [Description]    (hg19-Feb_2009)
EnsemblNAT9 - 17q25.1 [CytoView hg19]  NAT9 - 17q25.1 [CytoView hg38]
Mapping of homologs : NCBINAT9 [Mapview hg19]  NAT9 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK123115 AK225602 AK308569 AK312958 AL050269
RefSeq transcript (Entrez)NM_001305077 NM_001305078 NM_001305079 NM_001305080 NM_001305081 NM_001305082 NM_001305083 NM_001305084 NM_001305085 NM_001305086 NM_001305087 NM_001305088 NM_015654
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)NAT9
Cluster EST : UnigeneHs.144058 [ NCBI ]
CGAP (NCI)Hs.144058
Alternative Splicing GalleryENSG00000109065
Gene ExpressionNAT9 [ NCBI-GEO ]   NAT9 [ EBI - ARRAY_EXPRESS ]   NAT9 [ SEEK ]   NAT9 [ MEM ]
Gene Expression Viewer (FireBrowse)NAT9 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)26151
GTEX Portal (Tissue expression)NAT9
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9BTE0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9BTE0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9BTE0
Splice isoforms : SwissVarQ9BTE0
Catalytic activity : Enzyme2.3.1.- [ Enzyme-Expasy ]   2.3.1.-2.3.1.- [ IntEnz-EBI ]   2.3.1.- [ BRENDA ]   2.3.1.- [ KEGG ]   
PhosPhoSitePlusQ9BTE0
Domains : Interpro (EBI)Acyl_CoA_acyltransferase    GNAT_dom   
Domain families : Pfam (Sanger)Acetyltransf_3 (PF13302)   
Domain families : Pfam (NCBI)pfam13302   
Conserved Domain (NCBI)NAT9
DMDM Disease mutations26151
Blocks (Seattle)NAT9
SuperfamilyQ9BTE0
Human Protein AtlasENSG00000109065
Peptide AtlasQ9BTE0
HPRD13259
IPIIPI00003789   IPI00790050   
Protein Interaction databases
DIP (DOE-UCLA)Q9BTE0
IntAct (EBI)Q9BTE0
FunCoupENSG00000109065
BioGRIDNAT9
STRING (EMBL)NAT9
ZODIACNAT9
Ontologies - Pathways
QuickGOQ9BTE0
Ontology : AmiGOprotein binding  N-acetyltransferase activity  protein complex  
Ontology : EGO-EBIprotein binding  N-acetyltransferase activity  protein complex  
NDEx NetworkNAT9
Atlas of Cancer Signalling NetworkNAT9
Wikipedia pathwaysNAT9
Orthology - Evolution
OrthoDB26151
GeneTree (enSembl)ENSG00000109065
Phylogenetic Trees/Animal Genes : TreeFamNAT9
HOVERGENQ9BTE0
HOGENOMQ9BTE0
Homologs : HomoloGeneNAT9
Homology/Alignments : Family Browser (UCSC)NAT9
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerNAT9 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)NAT9
dbVarNAT9
ClinVarNAT9
1000_GenomesNAT9 
Exome Variant ServerNAT9
ExAC (Exome Aggregation Consortium)NAT9 (select the gene name)
Genetic variants : HAPMAP26151
Genomic Variants (DGV)NAT9 [DGVbeta]
DECIPHERNAT9 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisNAT9 
Mutations
ICGC Data PortalNAT9 
TCGA Data PortalNAT9 
Broad Tumor PortalNAT9
OASIS PortalNAT9 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICNAT9  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDNAT9
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 NAT9
DgiDB (Drug Gene Interaction Database)NAT9
DoCM (Curated mutations)NAT9 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)NAT9 (select a term)
intoGenNAT9
Cancer3DNAT9(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenNAT9
Genetic Testing Registry NAT9
NextProtQ9BTE0 [Medical]
TSGene26151
GENETestsNAT9
Target ValidationNAT9
Huge Navigator NAT9 [HugePedia]
snp3D : Map Gene to Disease26151
BioCentury BCIQNAT9
ClinGenNAT9
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD26151
Chemical/Pharm GKB GenePA142671281
Clinical trialNAT9
Miscellaneous
canSAR (ICR)NAT9 (select the gene name)
Probes
Litterature
PubMed18 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineNAT9
EVEXNAT9
GoPubMedNAT9
iHOPNAT9
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed May 31 15:32:17 CEST 2017

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