Atlas of Genetics and Cytogenetics in Oncology and Haematology


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NOTCH2NLB (notch 2 N-terminal like B)

Identity

Other aliasN2N
NOTCH2NL
NOTCH2NLA
HGNC (Hugo) NOTCH2NLB
LocusID (NCBI) 100996763
Atlas_Id 80625
Location 1q21.2  [Link to chromosome band 1q21]
Location_base_pair Starts at 148599807 and ends at 148679764 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
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


External links

Nomenclature
HGNC (Hugo)NOTCH2NLB   53923
Cards
Entrez_Gene (NCBI)NOTCH2NLB  100996763  notch 2 N-terminal like B
AliasesN2N; NOTCH2NL; NOTCH2NLA
GeneCards (Weizmann)NOTCH2NLB
Ensembl hg19 (Hinxton)ENSG00000270629 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000270629 [Gene_View]  ENSG00000270629 [Sequence]  chr1:148599807-148679764 [Contig_View]  NOTCH2NLB [Vega]
ICGC DataPortalENSG00000270629
TCGA cBioPortalNOTCH2NLB
AceView (NCBI)NOTCH2NLB
Genatlas (Paris)NOTCH2NLB
WikiGenes100996763
SOURCE (Princeton)NOTCH2NLB
Genetics Home Reference (NIH)NOTCH2NLB
Genomic and cartography
GoldenPath hg38 (UCSC)NOTCH2NLB  -     chr1:148599807-148679764 -  1q21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)NOTCH2NLB  -     1q21.2   [Description]    (hg19-Feb_2009)
GoldenPathNOTCH2NLB - 1q21.2 [CytoView hg19]  NOTCH2NLB - 1q21.2 [CytoView hg38]
ImmunoBaseENSG00000270629
Mapping of homologs : NCBINOTCH2NLB [Mapview hg19]  NOTCH2NLB [Mapview hg38]
OMIM618024   
Gene and transcription
Genbank (Entrez)MH721899
RefSeq transcript (Entrez)NM_001364007 NM_001364008
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)NOTCH2NLB
Alternative Splicing GalleryENSG00000270629
Gene ExpressionNOTCH2NLB [ NCBI-GEO ]   NOTCH2NLB [ EBI - ARRAY_EXPRESS ]   NOTCH2NLB [ SEEK ]   NOTCH2NLB [ MEM ]
Gene Expression Viewer (FireBrowse)NOTCH2NLB [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100996763
GTEX Portal (Tissue expression)NOTCH2NLB
Human Protein AtlasENSG00000270629-NOTCH2NLB [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)NOTCH2NLB
DMDM Disease mutations100996763
Blocks (Seattle)NOTCH2NLB
Human Protein Atlas [tissue]ENSG00000270629-NOTCH2NLB [tissue]
Protein Interaction databases
FunCoupENSG00000270629
BioGRIDNOTCH2NLB
STRING (EMBL)NOTCH2NLB
ZODIACNOTCH2NLB
Ontologies - Pathways
Huge Navigator NOTCH2NLB [HugePedia]
snp3D : Map Gene to Disease100996763
BioCentury BCIQNOTCH2NLB
ClinGenNOTCH2NLB
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100996763
Clinical trialNOTCH2NLB
Miscellaneous
canSAR (ICR)NOTCH2NLB (select the gene name)
DataMed IndexNOTCH2NLB
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineNOTCH2NLB
EVEXNOTCH2NLB
GoPubMedNOTCH2NLB
iHOPNOTCH2NLB
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Sep 3 15:57:58 CEST 2019

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