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SNORD31B (small nucleolar RNA, C/D box 31B)

Identity

Other alias-
HGNC (Hugo) SNORD31B
LocusID (NCBI) 109616978
Atlas_Id 80240
Location 13q33.3  [Link to chromosome band 13q33]
Location_base_pair Starts at 107320895 and ends at 107320963 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)SNORD31B   52226
Cards
Entrez_Gene (NCBI)SNORD31B  109616978  small nucleolar RNA, C/D box 31B
Aliases
GeneCards (Weizmann)SNORD31B
Ensembl hg19 (Hinxton)ENSG00000201847 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000201847 [Gene_View]  chr13:107320895-107320963 [Contig_View]  SNORD31B [Vega]
ICGC DataPortalENSG00000201847
TCGA cBioPortalSNORD31B
AceView (NCBI)SNORD31B
Genatlas (Paris)SNORD31B
WikiGenes109616978
SOURCE (Princeton)SNORD31B
Genetics Home Reference (NIH)SNORD31B
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD31B  -     chr13:107320895-107320963 -  13q33.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD31B  -     13q33.3   [Description]    (hg19-Feb_2009)
EnsemblSNORD31B - 13q33.3 [CytoView hg19]  SNORD31B - 13q33.3 [CytoView hg38]
Mapping of homologs : NCBISNORD31B [Mapview hg19]  SNORD31B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD31B
Alternative Splicing GalleryENSG00000201847
Gene ExpressionSNORD31B [ NCBI-GEO ]   SNORD31B [ EBI - ARRAY_EXPRESS ]   SNORD31B [ SEEK ]   SNORD31B [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD31B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)109616978
GTEX Portal (Tissue expression)SNORD31B
Human Protein AtlasENSG00000201847-SNORD31B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD31B
DMDM Disease mutations109616978
Blocks (Seattle)SNORD31B
Human Protein Atlas [tissue]ENSG00000201847-SNORD31B [tissue]
Protein Interaction databases
FunCoupENSG00000201847
BioGRIDSNORD31B
STRING (EMBL)SNORD31B
ZODIACSNORD31B
Ontologies - Pathways
Huge Navigator SNORD31B [HugePedia]
snp3D : Map Gene to Disease109616978
BioCentury BCIQSNORD31B
ClinGenSNORD31B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD109616978
Clinical trialSNORD31B
Miscellaneous
canSAR (ICR)SNORD31B (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD31B
EVEXSNORD31B
GoPubMedSNORD31B
iHOPSNORD31B
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 : Tue Nov 21 13:29:00 CET 2017

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