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NOSIP (nitric oxide synthase interacting protein)

Identity

Alias_symbol (synonym)CGI-25
Other alias
HGNC (Hugo) NOSIP
LocusID (NCBI) 51070
Atlas_Id 70909
Location 19q13.33  [Link to chromosome band 19q13]
Location_base_pair Starts at 50058725 and ends at 50083829 bp from pter ( according to hg19-Feb_2009)

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)NOSIP   17946
Cards
Entrez_Gene (NCBI)NOSIP  51070  nitric oxide synthase interacting protein
AliasesCGI-25
GeneCards (Weizmann)NOSIP
Ensembl hg19 (Hinxton)ENSG00000142546 [Gene_View]  chr19:50058725-50083829 [Contig_View]  NOSIP [Vega]
Ensembl hg38 (Hinxton)ENSG00000142546 [Gene_View]  chr19:50058725-50083829 [Contig_View]  NOSIP [Vega]
ICGC DataPortalENSG00000142546
TCGA cBioPortalNOSIP
AceView (NCBI)NOSIP
Genatlas (Paris)NOSIP
WikiGenes51070
SOURCE (Princeton)NOSIP
Genetics Home Reference (NIH)NOSIP
Genomic and cartography
GoldenPath hg19 (UCSC)NOSIP  -     chr19:50058725-50083829 -  19q13.33   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)NOSIP  -     19q13.33   [Description]    (hg38-Dec_2013)
EnsemblNOSIP - 19q13.33 [CytoView hg19]  NOSIP - 19q13.33 [CytoView hg38]
Mapping of homologs : NCBINOSIP [Mapview hg19]  NOSIP [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF132959 AK092444 AK291535 AK300720 BC009299
RefSeq transcript (Entrez)NM_001270960 NM_015953
RefSeq genomic (Entrez)NC_000019 NC_018930 NT_011109 NW_004929415
Consensus coding sequences : CCDS (NCBI)NOSIP
Cluster EST : UnigeneHs.7236 [ NCBI ]
CGAP (NCI)Hs.7236
Alternative Splicing GalleryENSG00000142546
Gene ExpressionNOSIP [ NCBI-GEO ]   NOSIP [ EBI - ARRAY_EXPRESS ]   NOSIP [ SEEK ]   NOSIP [ MEM ]
Gene Expression Viewer (FireBrowse)NOSIP [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)51070
GTEX Portal (Tissue expression)NOSIP
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9Y314   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9Y314  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9Y314
Splice isoforms : SwissVarQ9Y314
PhosPhoSitePlusQ9Y314
Domains : Interpro (EBI)Nitric_oxide_synth-interacting    Znf_RING/FYVE/PHD   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)NOSIP
DMDM Disease mutations51070
Blocks (Seattle)NOSIP
SuperfamilyQ9Y314
Human Protein AtlasENSG00000142546
Peptide AtlasQ9Y314
HPRD17642
IPIIPI00006408   IPI00910915   
Protein Interaction databases
DIP (DOE-UCLA)Q9Y314
IntAct (EBI)Q9Y314
FunCoupENSG00000142546
BioGRIDNOSIP
STRING (EMBL)NOSIP
ZODIACNOSIP
Ontologies - Pathways
QuickGOQ9Y314
Ontology : AmiGOGolgi membrane  protein binding  nucleus  nucleoplasm  cytoplasm  cytosol  negative regulation of catalytic activity  small molecule metabolic process  poly(A) RNA binding  nitric oxide metabolic process  regulation of nitric-oxide synthase activity  negative regulation of nitric-oxide synthase activity  
Ontology : EGO-EBIGolgi membrane  protein binding  nucleus  nucleoplasm  cytoplasm  cytosol  negative regulation of catalytic activity  small molecule metabolic process  poly(A) RNA binding  nitric oxide metabolic process  regulation of nitric-oxide synthase activity  negative regulation of nitric-oxide synthase activity  
NDEx NetworkNOSIP
Atlas of Cancer Signalling NetworkNOSIP
Wikipedia pathwaysNOSIP
Orthology - Evolution
OrthoDB51070
GeneTree (enSembl)ENSG00000142546
Phylogenetic Trees/Animal Genes : TreeFamNOSIP
HOVERGENQ9Y314
HOGENOMQ9Y314
Homologs : HomoloGeneNOSIP
Homology/Alignments : Family Browser (UCSC)NOSIP
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerNOSIP [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)NOSIP
dbVarNOSIP
ClinVarNOSIP
1000_GenomesNOSIP 
Exome Variant ServerNOSIP
ExAC (Exome Aggregation Consortium)NOSIP (select the gene name)
Genetic variants : HAPMAP51070
Genomic Variants (DGV)NOSIP [DGVbeta]
DECIPHER (Syndromes)19:50058725-50083829  ENSG00000142546
CONAN: Copy Number AnalysisNOSIP 
Mutations
ICGC Data PortalNOSIP 
TCGA Data PortalNOSIP 
Broad Tumor PortalNOSIP
OASIS PortalNOSIP [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICNOSIP  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDNOSIP
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch NOSIP
DgiDB (Drug Gene Interaction Database)NOSIP
DoCM (Curated mutations)NOSIP (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)NOSIP (select a term)
intoGenNOSIP
Cancer3DNOSIP(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenNOSIP
Genetic Testing Registry NOSIP
NextProtQ9Y314 [Medical]
TSGene51070
GENETestsNOSIP
Huge Navigator NOSIP [HugePedia]
snp3D : Map Gene to Disease51070
BioCentury BCIQNOSIP
ClinGenNOSIP
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD51070
Chemical/Pharm GKB GenePA134989259
Clinical trialNOSIP
Miscellaneous
canSAR (ICR)NOSIP (select the gene name)
Probes
Litterature
PubMed25 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineNOSIP
EVEXNOSIP
GoPubMedNOSIP
iHOPNOSIP
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Tue Mar 14 12:35:10 CET 2017

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