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SNORA30B (small nucleolar RNA, H/ACA box 30B)

Identity

Other alias-
HGNC (Hugo) SNORA30B
LocusID (NCBI) 109616992
Atlas_Id 79066
Location 9p21.3  [Link to chromosome band 9p21]
Location_base_pair Starts at 20786927 and ends at 20787055 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)SNORA30B   52200
Cards
Entrez_Gene (NCBI)SNORA30B  109616992  small nucleolar RNA, H/ACA box 30B
Aliases
GeneCards (Weizmann)SNORA30B
Ensembl hg19 (Hinxton)ENSG00000202189 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000202189 [Gene_View]  chr9:20786927-20787055 [Contig_View]  SNORA30B [Vega]
ICGC DataPortalENSG00000202189
TCGA cBioPortalSNORA30B
AceView (NCBI)SNORA30B
Genatlas (Paris)SNORA30B
WikiGenes109616992
SOURCE (Princeton)SNORA30B
Genetics Home Reference (NIH)SNORA30B
Genomic and cartography
GoldenPath hg38 (UCSC)SNORA30B  -     chr9:20786927-20787055 +  9p21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORA30B  -     9p21.3   [Description]    (hg19-Feb_2009)
EnsemblSNORA30B - 9p21.3 [CytoView hg19]  SNORA30B - 9p21.3 [CytoView hg38]
Mapping of homologs : NCBISNORA30B [Mapview hg19]  SNORA30B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORA30B
Alternative Splicing GalleryENSG00000202189
Gene ExpressionSNORA30B [ NCBI-GEO ]   SNORA30B [ EBI - ARRAY_EXPRESS ]   SNORA30B [ SEEK ]   SNORA30B [ MEM ]
Gene Expression Viewer (FireBrowse)SNORA30B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)109616992
GTEX Portal (Tissue expression)SNORA30B
Human Protein AtlasENSG00000202189-SNORA30B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORA30B
DMDM Disease mutations109616992
Blocks (Seattle)SNORA30B
Human Protein Atlas [tissue]ENSG00000202189-SNORA30B [tissue]
Protein Interaction databases
FunCoupENSG00000202189
BioGRIDSNORA30B
STRING (EMBL)SNORA30B
ZODIACSNORA30B
Ontologies - Pathways
Huge Navigator SNORA30B [HugePedia]
snp3D : Map Gene to Disease109616992
BioCentury BCIQSNORA30B
ClinGenSNORA30B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD109616992
Clinical trialSNORA30B
Miscellaneous
canSAR (ICR)SNORA30B (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORA30B
EVEXSNORA30B
GoPubMedSNORA30B
iHOPSNORA30B
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 : Tue Nov 21 13:20:42 CET 2017

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