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SNORD32B (small nucleolar RNA, C/D box 32B)

Identity

Alias_symbol (synonym)U32B
Other alias
HGNC (Hugo) SNORD32B
LocusID (NCBI) 692092
Atlas_Id 73934
Location 6p22.1  [Link to chromosome band 6p22]
Location_base_pair Starts at 29582252 and ends at 29582328 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)SNORD32B   32719
Cards
Entrez_Gene (NCBI)SNORD32B  692092  small nucleolar RNA, C/D box 32B
AliasesU32B
GeneCards (Weizmann)SNORD32B
Ensembl hg19 (Hinxton)ENSG00000201330 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000201330 [Gene_View]  chr6:29582252-29582328 [Contig_View]  SNORD32B [Vega]
ICGC DataPortalENSG00000201330
TCGA cBioPortalSNORD32B
AceView (NCBI)SNORD32B
Genatlas (Paris)SNORD32B
WikiGenes692092
SOURCE (Princeton)SNORD32B
Genetics Home Reference (NIH)SNORD32B
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD32B  -     chr6:29582252-29582328 +  6p22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD32B  -     6p22.1   [Description]    (hg19-Feb_2009)
EnsemblSNORD32B - 6p22.1 [CytoView hg19]  SNORD32B - 6p22.1 [CytoView hg38]
Mapping of homologs : NCBISNORD32B [Mapview hg19]  SNORD32B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000006 NC_018917 NT_113891 NT_167244 NT_167245 NT_167246 NT_167247 NT_167248
Consensus coding sequences : CCDS (NCBI)SNORD32B
Alternative Splicing GalleryENSG00000201330
Gene ExpressionSNORD32B [ NCBI-GEO ]   SNORD32B [ EBI - ARRAY_EXPRESS ]   SNORD32B [ SEEK ]   SNORD32B [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD32B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)692092
GTEX Portal (Tissue expression)SNORD32B
Human Protein AtlasENSG00000201330-SNORD32B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD32B
DMDM Disease mutations692092
Blocks (Seattle)SNORD32B
Human Protein Atlas [tissue]ENSG00000201330-SNORD32B [tissue]
Protein Interaction databases
FunCoupENSG00000201330
BioGRIDSNORD32B
STRING (EMBL)SNORD32B
ZODIACSNORD32B
Ontologies - Pathways
Huge Navigator SNORD32B [HugePedia]
snp3D : Map Gene to Disease692092
BioCentury BCIQSNORD32B
ClinGenSNORD32B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD692092
Chemical/Pharm GKB GenePA145007800
Clinical trialSNORD32B
Miscellaneous
canSAR (ICR)SNORD32B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD32B
EVEXSNORD32B
GoPubMedSNORD32B
iHOPSNORD32B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Fri Feb 23 18:53:31 CET 2018

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