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SNORD26 (small nucleolar RNA, C/D box 26)

Identity

Alias_namesRNU26
RNA, U26 small nucleolar
Alias_symbol (synonym)U26
Other alias
HGNC (Hugo) SNORD26
LocusID (NCBI) 9302
Atlas_Id 73927
Location 11q12.3  [Link to chromosome band 11q12]
Location_base_pair Starts at 62622764 and ends at 62622838 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)SNORD26   10148
Cards
Entrez_Gene (NCBI)SNORD26  9302  small nucleolar RNA, C/D box 26
AliasesRNU26; U26
GeneCards (Weizmann)SNORD26
Ensembl hg19 (Hinxton)ENSG00000276788 [Gene_View]  chr11:62622764-62622838 [Contig_View]  SNORD26 [Vega]
Ensembl hg38 (Hinxton)ENSG00000276788 [Gene_View]  chr11:62622764-62622838 [Contig_View]  SNORD26 [Vega]
ICGC DataPortalENSG00000276788
TCGA cBioPortalSNORD26
AceView (NCBI)SNORD26
Genatlas (Paris)SNORD26
WikiGenes9302
SOURCE (Princeton)SNORD26
Genetics Home Reference (NIH)SNORD26
Genomic and cartography
GoldenPath hg19 (UCSC)SNORD26  -     chr11:62622764-62622838 -  11q12.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)SNORD26  -     11q12.3   [Description]    (hg38-Dec_2013)
EnsemblSNORD26 - 11q12.3 [CytoView hg19]  SNORD26 - 11q12.3 [CytoView hg38]
Mapping of homologs : NCBISNORD26 [Mapview hg19]  SNORD26 [Mapview hg38]
OMIM603225   
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000011 NC_018922 NT_167190 NW_004929380
Consensus coding sequences : CCDS (NCBI)SNORD26
Alternative Splicing GalleryENSG00000276788
Gene ExpressionSNORD26 [ NCBI-GEO ]   SNORD26 [ EBI - ARRAY_EXPRESS ]   SNORD26 [ SEEK ]   SNORD26 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD26 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)9302
GTEX Portal (Tissue expression)SNORD26
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD26
DMDM Disease mutations9302
Blocks (Seattle)SNORD26
Human Protein AtlasENSG00000276788
Protein Interaction databases
FunCoupENSG00000276788
BioGRIDSNORD26
STRING (EMBL)SNORD26
ZODIACSNORD26
Ontologies - Pathways
Huge Navigator SNORD26 [HugePedia]
snp3D : Map Gene to Disease9302
BioCentury BCIQSNORD26
ClinGenSNORD26
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD9302
Chemical/Pharm GKB GenePA34514
Clinical trialSNORD26
Miscellaneous
canSAR (ICR)SNORD26 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD26
EVEXSNORD26
GoPubMedSNORD26
iHOPSNORD26
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Mar 14 12:45:40 CET 2017

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