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SNORD58B (small nucleolar RNA, C/D box 58B)

Identity

Alias_namesRNU58B
RNA, U58B small nuclear
Alias_symbol (synonym)U58b
Other alias
HGNC (Hugo) SNORD58B
LocusID (NCBI) 26790
Atlas_Id 73971
Location 18q21.1  [Link to chromosome band 18q21]
Location_base_pair Starts at 47018034 and ends at 47018099 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)SNORD58B   10209
Cards
Entrez_Gene (NCBI)SNORD58B  26790  small nucleolar RNA, C/D box 58B
AliasesRNU58B; U58b
GeneCards (Weizmann)SNORD58B
Ensembl hg19 (Hinxton)ENSG00000271982 [Gene_View]  chr18:47018034-47018099 [Contig_View]  SNORD58B [Vega]
Ensembl hg38 (Hinxton)ENSG00000271982 [Gene_View]  chr18:47018034-47018099 [Contig_View]  SNORD58B [Vega]
ICGC DataPortalENSG00000271982
TCGA cBioPortalSNORD58B
AceView (NCBI)SNORD58B
Genatlas (Paris)SNORD58B
WikiGenes26790
SOURCE (Princeton)SNORD58B
Genetics Home Reference (NIH)SNORD58B
Genomic and cartography
GoldenPath hg19 (UCSC)SNORD58B  -     chr18:47018034-47018099 -  18q21.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)SNORD58B  -     18q21.1   [Description]    (hg38-Dec_2013)
EnsemblSNORD58B - 18q21.1 [CytoView hg19]  SNORD58B - 18q21.1 [CytoView hg38]
Mapping of homologs : NCBISNORD58B [Mapview hg19]  SNORD58B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000018 NC_018929 NT_010966 NW_004929410
Consensus coding sequences : CCDS (NCBI)SNORD58B
Alternative Splicing GalleryENSG00000271982
Gene ExpressionSNORD58B [ NCBI-GEO ]   SNORD58B [ EBI - ARRAY_EXPRESS ]   SNORD58B [ SEEK ]   SNORD58B [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD58B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)26790
GTEX Portal (Tissue expression)SNORD58B
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD58B
DMDM Disease mutations26790
Blocks (Seattle)SNORD58B
Human Protein AtlasENSG00000271982
Protein Interaction databases
FunCoupENSG00000271982
BioGRIDSNORD58B
STRING (EMBL)SNORD58B
ZODIACSNORD58B
Ontologies - Pathways
Huge Navigator SNORD58B [HugePedia]
snp3D : Map Gene to Disease26790
BioCentury BCIQSNORD58B
ClinGenSNORD58B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD26790
Chemical/Pharm GKB GenePA34576
Clinical trialSNORD58B
Miscellaneous
canSAR (ICR)SNORD58B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD58B
EVEXSNORD58B
GoPubMedSNORD58B
iHOPSNORD58B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:45:49 CET 2017

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