SNORD115-26 (small nucleolar RNA, C/D box 115-26)

1. Identity

Alias_symbol (synonym)
General Information
Other alias
HGNC (Hugo) SNORD115-26
LocusID (NCBI) 100033802
Atlas_Id 73832
Location 15q11.2  [Link to chromosome band 15q11]
Location_base_pair Starts at 25218617 and ends at 25218698 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)

2. DNA/RNA

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

 


3. External links

Nomenclature
HGNC (Hugo)SNORD115-26   33045
Cards
Entrez_Gene (NCBI)SNORD115-26  100033802  small nucleolar RNA, C/D box 115-26
AliasesHBII-52-26
GeneCards (Weizmann)SNORD115-26
Ensembl hg19 (Hinxton)ENSG00000275524 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000275524 [Gene_View] &nbspENSG00000275524 [Sequence]  chr15:25218617-25218698 [Contig_View]  SNORD115-26 [Vega]
ICGC DataPortalENSG00000275524
TCGA cBioPortalSNORD115-26
AceView (NCBI)SNORD115-26
Genatlas (Paris)SNORD115-26
WikiGenes100033802
SOURCE (Princeton)SNORD115-26
Genetics Home Reference (NIH)SNORD115-26
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD115-26  -     chr15:25218617-25218698 +  15q11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD115-26  -     15q11.2   [Description]    (hg19-Feb_2009)
EnsemblSNORD115-26 - 15q11.2 [CytoView hg19]  SNORD115-26 - 15q11.2 [CytoView hg38]
Mapping of homologs : NCBISNORD115-26 [Mapview hg19]  SNORD115-26 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD115-26
Alternative Splicing GalleryENSG00000275524
Gene ExpressionSNORD115-26 [ NCBI-GEO ]   SNORD115-26 [ EBI - ARRAY_EXPRESS ]   SNORD115-26 [ SEEK ]   SNORD115-26 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD115-26 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets] &nbsp [Normal Tissue Atlas] &nbsp[carcinoma Classsification] &nbsp[NCI60]
BioGPS (Tissue expression)100033802
GTEX Portal (Tissue expression)SNORD115-26
Human Protein AtlasENSG00000275524-SNORD115-26 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD115-26
DMDM Disease mutations100033802
Blocks (Seattle)SNORD115-26
Human Protein Atlas [tissue]ENSG00000275524-SNORD115-26 [tissue]
Protein Interaction databases
FunCoupENSG00000275524
BioGRIDSNORD115-26
STRING (EMBL)SNORD115-26
ZODIACSNORD115-26
Ontologies - Pathways
Huge Navigator SNORD115-26 [HugePedia]
snp3D : Map Gene to Disease100033802
BioCentury BCIQSNORD115-26
ClinGenSNORD115-26
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100033802
Chemical/Pharm GKB GenePA162404231
Clinical trialSNORD115-26
Miscellaneous
canSAR (ICR)SNORD115-26 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD115-26
EVEXSNORD115-26
GoPubMedSNORD115-26
iHOPSNORD115-26
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Jul 30 14:31:21 CEST 2018

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