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SNORD63B (small nucleolar RNA, C/D box 63B)

Identity

Other alias-
HGNC (Hugo) SNORD63B
LocusID (NCBI) 109617013
Atlas_Id 79542
Location 5q31.2  [Link to chromosome band 5q31]
Location_base_pair Starts at 138558969 and ends at 138559041 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)SNORD63B   52230
Cards
Entrez_Gene (NCBI)SNORD63B  109617013  small nucleolar RNA, C/D box 63B
Aliases
GeneCards (Weizmann)SNORD63B
Ensembl hg19 (Hinxton)ENSG00000222937 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000222937 [Gene_View]  ENSG00000222937 [Sequence]  chr5:138558969-138559041 [Contig_View]  SNORD63B [Vega]
ICGC DataPortalENSG00000222937
TCGA cBioPortalSNORD63B
AceView (NCBI)SNORD63B
Genatlas (Paris)SNORD63B
WikiGenes109617013
SOURCE (Princeton)SNORD63B
Genetics Home Reference (NIH)SNORD63B
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD63B  -     chr5:138558969-138559041 -  5q31.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD63B  -     5q31.2   [Description]    (hg19-Feb_2009)
EnsemblSNORD63B - 5q31.2 [CytoView hg19]  SNORD63B - 5q31.2 [CytoView hg38]
Mapping of homologs : NCBISNORD63B [Mapview hg19]  SNORD63B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD63B
Alternative Splicing GalleryENSG00000222937
Gene ExpressionSNORD63B [ NCBI-GEO ]   SNORD63B [ EBI - ARRAY_EXPRESS ]   SNORD63B [ SEEK ]   SNORD63B [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD63B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)109617013
GTEX Portal (Tissue expression)SNORD63B
Human Protein AtlasENSG00000222937-SNORD63B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD63B
DMDM Disease mutations109617013
Blocks (Seattle)SNORD63B
Human Protein Atlas [tissue]ENSG00000222937-SNORD63B [tissue]
Protein Interaction databases
FunCoupENSG00000222937
BioGRIDSNORD63B
STRING (EMBL)SNORD63B
ZODIACSNORD63B
Ontologies - Pathways
Huge Navigator SNORD63B [HugePedia]
snp3D : Map Gene to Disease109617013
BioCentury BCIQSNORD63B
ClinGenSNORD63B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD109617013
Clinical trialSNORD63B
Miscellaneous
canSAR (ICR)SNORD63B (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD63B
EVEXSNORD63B
GoPubMedSNORD63B
iHOPSNORD63B
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 : Mon Jul 30 14:32:12 CEST 2018

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