Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

NOA1 (nitric oxide associated 1)

Identity

Alias_namesC4orf14
chromosome 4 open reading frame 14
Alias_symbol (synonym)MGC3232
hAtNOS1
hNOA1
MTG3
Other aliasmAtNOS1
HGNC (Hugo) NOA1
LocusID (NCBI) 84273
Atlas_Id 70893
Location 4q12  [Link to chromosome band 4q12]
Location_base_pair Starts at 56963344 and ends at 56977660 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
ARHGAP24 (4q21.23) / NOA1 (4q12)NOA1 (4q12) / N4BP1 (16q12.1)NOA1 (4q12) / PPP3CA (4q24)

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)NOA1   28473
Cards
Entrez_Gene (NCBI)NOA1  84273  nitric oxide associated 1
AliasesC4orf14; MTG3; hAtNOS1; hNOA1; 
mAtNOS1
GeneCards (Weizmann)NOA1
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr4:56963344-56977660 [Contig_View]  NOA1 [Vega]
TCGA cBioPortalNOA1
AceView (NCBI)NOA1
Genatlas (Paris)NOA1
WikiGenes84273
SOURCE (Princeton)NOA1
Genetics Home Reference (NIH)NOA1
Genomic and cartography
GoldenPath hg38 (UCSC)NOA1  -     chr4:56963344-56977660 -  4q12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)NOA1  -     4q12   [Description]    (hg19-Feb_2009)
EnsemblNOA1 - 4q12 [CytoView hg19]  NOA1 - 4q12 [CytoView hg38]
Mapping of homologs : NCBINOA1 [Mapview hg19]  NOA1 [Mapview hg38]
OMIM614919   
Gene and transcription
Genbank (Entrez)AA431879 AK074953 AK098215 AK128696 BC004894
RefSeq transcript (Entrez)NM_032313
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)NOA1
Cluster EST : UnigeneHs.8715 [ NCBI ]
CGAP (NCI)Hs.8715
Gene ExpressionNOA1 [ NCBI-GEO ]   NOA1 [ EBI - ARRAY_EXPRESS ]   NOA1 [ SEEK ]   NOA1 [ MEM ]
Gene Expression Viewer (FireBrowse)NOA1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)84273
GTEX Portal (Tissue expression)NOA1
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8NC60   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8NC60  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8NC60
Splice isoforms : SwissVarQ8NC60
PhosPhoSitePlusQ8NC60
Domaine pattern : Prosite (Expaxy)G_CP (PS51721)   
Domains : Interpro (EBI)G_CP_dom    GTP_binding_domain    P-loop_NTPase   
Domain families : Pfam (Sanger)MMR_HSR1 (PF01926)   
Domain families : Pfam (NCBI)pfam01926   
Conserved Domain (NCBI)NOA1
DMDM Disease mutations84273
Blocks (Seattle)NOA1
SuperfamilyQ8NC60
Peptide AtlasQ8NC60
HPRD12823
IPIIPI00385928   
Protein Interaction databases
DIP (DOE-UCLA)Q8NC60
IntAct (EBI)Q8NC60
BioGRIDNOA1
STRING (EMBL)NOA1
ZODIACNOA1
Ontologies - Pathways
QuickGOQ8NC60
Ontology : AmiGORNA binding  protein binding  GTP binding  mitochondrion  apoptotic process  regulation of cell death  extrinsic component of mitochondrial inner membrane  mitochondrial translation  regulation of cellular respiration  
Ontology : EGO-EBIRNA binding  protein binding  GTP binding  mitochondrion  apoptotic process  regulation of cell death  extrinsic component of mitochondrial inner membrane  mitochondrial translation  regulation of cellular respiration  
NDEx NetworkNOA1
Atlas of Cancer Signalling NetworkNOA1
Wikipedia pathwaysNOA1
Orthology - Evolution
OrthoDB84273
Phylogenetic Trees/Animal Genes : TreeFamNOA1
HOVERGENQ8NC60
HOGENOMQ8NC60
Homologs : HomoloGeneNOA1
Homology/Alignments : Family Browser (UCSC)NOA1
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerNOA1 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)NOA1
dbVarNOA1
ClinVarNOA1
1000_GenomesNOA1 
Exome Variant ServerNOA1
ExAC (Exome Aggregation Consortium)NOA1 (select the gene name)
Genetic variants : HAPMAP84273
Genomic Variants (DGV)NOA1 [DGVbeta]
DECIPHERNOA1 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisNOA1 
Mutations
ICGC Data PortalNOA1 
TCGA Data PortalNOA1 
Broad Tumor PortalNOA1
OASIS PortalNOA1 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDNOA1
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 NOA1
DgiDB (Drug Gene Interaction Database)NOA1
DoCM (Curated mutations)NOA1 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)NOA1 (select a term)
intoGenNOA1
Cancer3DNOA1(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM614919   
Orphanet
MedgenNOA1
Genetic Testing Registry NOA1
NextProtQ8NC60 [Medical]
TSGene84273
GENETestsNOA1
Target ValidationNOA1
Huge Navigator NOA1 [HugePedia]
snp3D : Map Gene to Disease84273
BioCentury BCIQNOA1
ClinGenNOA1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD84273
Chemical/Pharm GKB GenePA134878853
Clinical trialNOA1
Miscellaneous
canSAR (ICR)NOA1 (select the gene name)
Probes
Litterature
PubMed20 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineNOA1
EVEXNOA1
GoPubMedNOA1
iHOPNOA1
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Wed May 31 15:32:50 CEST 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.