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SNORD11B (small nucleolar RNA, C/D box 11B)

Identity

Other alias-
HGNC (Hugo) SNORD11B
LocusID (NCBI) 100113392
Atlas_Id 73895
Location 2q33.1  [Link to chromosome band 2q33]
Location_base_pair Starts at 202291317 and ends at 202291428 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)SNORD11B   33571
Cards
Entrez_Gene (NCBI)SNORD11B  100113392  small nucleolar RNA, C/D box 11B
Aliases
GeneCards (Weizmann)SNORD11B
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr2:202291317-202291428 [Contig_View]  SNORD11B [Vega]
TCGA cBioPortalSNORD11B
AceView (NCBI)SNORD11B
Genatlas (Paris)SNORD11B
WikiGenes100113392
SOURCE (Princeton)SNORD11B
Genetics Home Reference (NIH)SNORD11B
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD11B  -     chr2:202291317-202291428 +  2q33.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD11B  -     2q33.1   [Description]    (hg19-Feb_2009)
EnsemblSNORD11B - 2q33.1 [CytoView hg19]  SNORD11B - 2q33.1 [CytoView hg38]
Mapping of homologs : NCBISNORD11B [Mapview hg19]  SNORD11B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD11B
Cluster EST : UnigeneHs.693442 [ NCBI ]
CGAP (NCI)Hs.693442
Gene ExpressionSNORD11B [ NCBI-GEO ]   SNORD11B [ EBI - ARRAY_EXPRESS ]   SNORD11B [ SEEK ]   SNORD11B [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD11B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100113392
GTEX Portal (Tissue expression)SNORD11B
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD11B
DMDM Disease mutations100113392
Blocks (Seattle)SNORD11B
Protein Interaction databases
BioGRIDSNORD11B
STRING (EMBL)SNORD11B
ZODIACSNORD11B
Ontologies - Pathways
Huge Navigator SNORD11B [HugePedia]
snp3D : Map Gene to Disease100113392
BioCentury BCIQSNORD11B
ClinGenSNORD11B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100113392
Chemical/Pharm GKB GenePA162404286
Clinical trialSNORD11B
Miscellaneous
canSAR (ICR)SNORD11B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD11B
EVEXSNORD11B
GoPubMedSNORD11B
iHOPSNORD11B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Nov 9 12:29:30 CET 2017

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