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NBPF26 (NBPF member 26)

Identity

Alias_namesneuroblastoma breakpoint family
Other alias-
HGNC (Hugo) NBPF26
LocusID (NCBI) 101060684
Atlas_Id 56575
Location 1p11.2  [Link to chromosome band 1p11]
Location_base_pair Starts at 120451180 and ends at 120840911 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


External links

Nomenclature
HGNC (Hugo)NBPF26   49571
Cards
Entrez_Gene (NCBI)NBPF26  101060684  NBPF member 26
Aliases
GeneCards (Weizmann)NBPF26
Ensembl hg19 (Hinxton)ENSG00000273136 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000273136 [Gene_View]  chr1:120451180-120840911 [Contig_View]  NBPF26 [Vega]
ICGC DataPortalENSG00000273136
TCGA cBioPortalNBPF26
AceView (NCBI)NBPF26
Genatlas (Paris)NBPF26
WikiGenes101060684
SOURCE (Princeton)NBPF26
Genetics Home Reference (NIH)NBPF26
Genomic and cartography
GoldenPath hg38 (UCSC)NBPF26  -     chr1:120451180-120840911 +  1p11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)NBPF26  -     1p11.2   [Description]    (hg19-Feb_2009)
EnsemblNBPF26 - 1p11.2 [CytoView hg19]  NBPF26 - 1p11.2 [CytoView hg38]
Mapping of homologs : NCBINBPF26 [Mapview hg19]  NBPF26 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK294944 AW965356 DA203219 DA675097
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)NBPF26
Cluster EST : UnigeneHs.714127 [ NCBI ]
CGAP (NCI)Hs.714127
Alternative Splicing GalleryENSG00000273136
Gene ExpressionNBPF26 [ NCBI-GEO ]   NBPF26 [ EBI - ARRAY_EXPRESS ]   NBPF26 [ SEEK ]   NBPF26 [ MEM ]
Gene Expression Viewer (FireBrowse)NBPF26 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)101060684
GTEX Portal (Tissue expression)NBPF26
Protein : pattern, domain, 3D structure
UniProt/SwissProtB4DH59   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtB4DH59  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProB4DH59
Splice isoforms : SwissVarB4DH59
PhosPhoSitePlusB4DH59
Domaine pattern : Prosite (Expaxy)NBPF (PS51316)   
Domains : Interpro (EBI)NBPF_dom   
Domain families : Pfam (Sanger)DUF1220 (PF06758)   
Domain families : Pfam (NCBI)pfam06758   
Domain families : Smart (EMBL)DUF1220 (SM01148)  
Conserved Domain (NCBI)NBPF26
DMDM Disease mutations101060684
Blocks (Seattle)NBPF26
SuperfamilyB4DH59
Human Protein AtlasENSG00000273136
Peptide AtlasB4DH59
Protein Interaction databases
DIP (DOE-UCLA)B4DH59
IntAct (EBI)B4DH59
FunCoupENSG00000273136
BioGRIDNBPF26
STRING (EMBL)NBPF26
ZODIACNBPF26
Ontologies - Pathways
QuickGOB4DH59
Ontology : AmiGOcytoplasm  
Ontology : EGO-EBIcytoplasm  
NDEx NetworkNBPF26
Atlas of Cancer Signalling NetworkNBPF26
Wikipedia pathwaysNBPF26
Orthology - Evolution
OrthoDB101060684
GeneTree (enSembl)ENSG00000273136
Phylogenetic Trees/Animal Genes : TreeFamNBPF26
HOVERGENB4DH59
HOGENOMB4DH59
Homologs : HomoloGeneNBPF26
Homology/Alignments : Family Browser (UCSC)NBPF26
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerNBPF26 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)NBPF26
dbVarNBPF26
ClinVarNBPF26
1000_GenomesNBPF26 
Exome Variant ServerNBPF26
ExAC (Exome Aggregation Consortium)NBPF26 (select the gene name)
Genetic variants : HAPMAP101060684
Genomic Variants (DGV)NBPF26 [DGVbeta]
DECIPHERNBPF26 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisNBPF26 
Mutations
ICGC Data PortalNBPF26 
TCGA Data PortalNBPF26 
Broad Tumor PortalNBPF26
OASIS PortalNBPF26 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDNBPF26
BioMutasearch NBPF26
DgiDB (Drug Gene Interaction Database)NBPF26
DoCM (Curated mutations)NBPF26 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)NBPF26 (select a term)
intoGenNBPF26
Cancer3DNBPF26(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenNBPF26
Genetic Testing Registry NBPF26
NextProtB4DH59 [Medical]
TSGene101060684
GENETestsNBPF26
Target ValidationNBPF26
Huge Navigator NBPF26 [HugePedia]
snp3D : Map Gene to Disease101060684
BioCentury BCIQNBPF26
ClinGenNBPF26
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101060684
Chemical/Pharm GKB GenePA166123706
Clinical trialNBPF26
Miscellaneous
canSAR (ICR)NBPF26 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineNBPF26
EVEXNBPF26
GoPubMedNBPF26
iHOPNBPF26
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 25 19:21:32 CEST 2017

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