Atlas of Genetics and Cytogenetics in Oncology and Haematology

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NRSN2 (neurensin 2)

Identity

Other namesC20orf98
dJ1103G7.6
HGNC (Hugo) NRSN2
LocusID (NCBI) 80023
Location 20p13
Location_base_pair Starts at 327370 and ends at 335512 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)NRSN2   16229
Entrez_Gene (NCBI)NRSN2  80023  neurensin 2
Cards
GeneCards (Weizmann)NRSN2
Ensembl (Hinxton)ENSG00000125841 [Gene_View]  chr20:327370-335512 [Contig_View]  NRSN2 [Vega]
AceView (NCBI)NRSN2
Genatlas (Paris)NRSN2
SOURCE (Stanford)NM_024958
Genomic and cartography
GoldenPath (UCSC)NRSN2  -  20p13   chr20:327370-335512 +  20p13   [Description]    (hg19-Feb_2009)
EnsemblNRSN2 - 20p13 [CytoView]
Mapping of homologs : NCBINRSN2 [Mapview]
OMIM610666   
Gene and transcription
Genbank (Entrez)AK026982 AK290527 AL136915 AM393375 AW292804
RefSeq transcript (SRS)NM_024958
RefSeq transcript (Entrez)NM_024958
RefSeq genomic (SRS)AC_000152 NC_000020 NC_018931 NT_011387 NW_001838652 NW_004078100
RefSeq genomic (Entrez)AC_000152 NC_000020 NC_018931 NT_011387 NW_001838652 NW_004078100
Consensus coding sequences : CCDS (NCBI)NRSN2
Cluster EST : UnigeneHs.416024 [ SRS ] Hs.416024 [ NCBI ]
CGAP (NCI)Hs.416024
Alternative Splicing : Fast-db (Paris)GSHG0018494
Alternative Splicing GalleryENSG00000125841
Gene ExpressionNRSN2 [ NCBI-GEO ]   NRSN2 [ EBI - ARRAY_EXPRESS ]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9GZP1 (SRS) Q9GZP1 (Uniprot)
NextProtQ9GZP1
With graphics : InterProQ9GZP1
Splice isoforms : SwissVarQ9GZP1(Swissvar)
Domains : Interpro (SRS)Neurensin   
Domains : Interpro (EBI)Neurensin   
Related proteins : CluSTrQ9GZP1
Domain families : Pfam (SRS)
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
DMDM80023
Blocks (Seattle)Q9GZP1
Human Protein AtlasENSG00000125841
HPRD12791
IPIIPI00017231   
Protein Interaction databases
DIP (DOE-UCLA)Q9GZP1
IntAct (EBI)Q9GZP1
FunCoupENSG00000125841
REACTOMENRSN2
Protein Interaction Database80023
BioGRIDNRSN2
InParanoidQ9GZP1
Interologous Interaction database Q9GZP1
IntegromeDBNRSN2
Polymorphism : SNP, mutations, diseases
SNP Single Nucleotide Polymorphism (NCBI)NRSN2
SNP (GeneSNP Utah)NRSN2
SNP : HGBaseNRSN2
Genetic variants : HAPMAPNRSN2
Somatic Mutations in Cancer : COSMICNRSN2 
CONAN: Copy Number AnalysisNRSN2 
Mutations and Diseases : HGMDNRSN2
OMIM610666   
GENETests610666   
Disease Genetic AssociationNRSN2
Huge Navigator NRSN2 [HugePedia]  NRSN2 [HugeCancerGEM]
Genomic VariantsNRSN2  NRSN2 [DGVbeta]
ClinVarNRSN2
snp3D : Map Gene to Disease80023
General knowledge
Homologs : HomoloGeneNRSN2
Homology/Alignments : Family Browser (UCSC)NRSN2
Phylogenetic Trees/Animal Genes : TreeFamNRSN2
Chemical/Protein Interactions : CTD80023
Chemical/Pharm GKB GenePA25805
Clinical trialNRSN2
Cancer Resource (Charite)ENSG00000125841
Ontology : AmiGOmolecular_function  plasma membrane  biological_process  integral to membrane  transport vesicle  neuronal cell body  
Ontology : EGO-EBImolecular_function  plasma membrane  biological_process  integral to membrane  transport vesicle  neuronal cell body  
Other databases
Probes
Litterature
PubMed16 Pubmed reference(s) in Entrez
PubGeneNRSN2
iHOPNRSN2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

Contributor(s)

Written09-2002Dessen P, Le Minor S
Updated01-2013Dessen P

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Fri Jun 14 17:29:00 CEST 2013
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