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SNORD30 (small nucleolar RNA, C/D box 30)

Identity

Alias_namesRNU30
RNA, U30 small nucleolar
Alias_symbol (synonym)U30
Other alias
HGNC (Hugo) SNORD30
LocusID (NCBI) 9299
Atlas_Id 73931
Location 11q12.3  [Link to chromosome band 11q12]
Location_base_pair Starts at 62621135 and ends at 62621204 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)SNORD30   10157
Cards
Entrez_Gene (NCBI)SNORD30  9299  small nucleolar RNA, C/D box 30
AliasesRNU30; U30
GeneCards (Weizmann)SNORD30
Ensembl hg19 (Hinxton)ENSG00000277846 [Gene_View]  chr11:62621135-62621204 [Contig_View]  SNORD30 [Vega]
Ensembl hg38 (Hinxton)ENSG00000277846 [Gene_View]  chr11:62621135-62621204 [Contig_View]  SNORD30 [Vega]
ICGC DataPortalENSG00000277846
TCGA cBioPortalSNORD30
AceView (NCBI)SNORD30
Genatlas (Paris)SNORD30
WikiGenes9299
SOURCE (Princeton)SNORD30
Genetics Home Reference (NIH)SNORD30
Genomic and cartography
GoldenPath hg19 (UCSC)SNORD30  -     chr11:62621135-62621204 -  11q12.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)SNORD30  -     11q12.3   [Description]    (hg38-Dec_2013)
EnsemblSNORD30 - 11q12.3 [CytoView hg19]  SNORD30 - 11q12.3 [CytoView hg38]
Mapping of homologs : NCBISNORD30 [Mapview hg19]  SNORD30 [Mapview hg38]
OMIM603229   
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000011 NC_018922 NT_167190 NW_004929380
Consensus coding sequences : CCDS (NCBI)SNORD30
Alternative Splicing GalleryENSG00000277846
Gene ExpressionSNORD30 [ NCBI-GEO ]   SNORD30 [ EBI - ARRAY_EXPRESS ]   SNORD30 [ SEEK ]   SNORD30 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD30 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)9299
GTEX Portal (Tissue expression)SNORD30
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD30
DMDM Disease mutations9299
Blocks (Seattle)SNORD30
Human Protein AtlasENSG00000277846
Protein Interaction databases
FunCoupENSG00000277846
BioGRIDSNORD30
STRING (EMBL)SNORD30
ZODIACSNORD30
Ontologies - Pathways
Huge Navigator SNORD30 [HugePedia]
snp3D : Map Gene to Disease9299
BioCentury BCIQSNORD30
ClinGenSNORD30
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD9299
Chemical/Pharm GKB GenePA34523
Clinical trialSNORD30
Miscellaneous
canSAR (ICR)SNORD30 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD30
EVEXSNORD30
GoPubMedSNORD30
iHOPSNORD30
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 Mar 14 12:45:41 CET 2017

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