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SNORD3G (small nucleolar RNA, C/D box 3G)

Identity

Other alias-
HGNC (Hugo) SNORD3G
LocusID (NCBI) 109616984
Atlas_Id 79565
Location 1p22.2  [Link to chromosome band 1p22]
Location_base_pair Starts at 90657750 and ends at 90657963 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)SNORD3G   52240
Cards
Entrez_Gene (NCBI)SNORD3G  109616984  small nucleolar RNA, C/D box 3G
Aliases
GeneCards (Weizmann)SNORD3G
Ensembl hg19 (Hinxton)ENSG00000199666 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000199666 [Gene_View]  chr1:90657750-90657963 [Contig_View]  SNORD3G [Vega]
ICGC DataPortalENSG00000199666
TCGA cBioPortalSNORD3G
AceView (NCBI)SNORD3G
Genatlas (Paris)SNORD3G
WikiGenes109616984
SOURCE (Princeton)SNORD3G
Genetics Home Reference (NIH)SNORD3G
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD3G  -     chr1:90657750-90657963 +  1p22.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD3G  -     1p22.2   [Description]    (hg19-Feb_2009)
EnsemblSNORD3G - 1p22.2 [CytoView hg19]  SNORD3G - 1p22.2 [CytoView hg38]
Mapping of homologs : NCBISNORD3G [Mapview hg19]  SNORD3G [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD3G
Alternative Splicing GalleryENSG00000199666
Gene ExpressionSNORD3G [ NCBI-GEO ]   SNORD3G [ EBI - ARRAY_EXPRESS ]   SNORD3G [ SEEK ]   SNORD3G [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD3G [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)109616984
GTEX Portal (Tissue expression)SNORD3G
Human Protein AtlasENSG00000199666-SNORD3G [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD3G
DMDM Disease mutations109616984
Blocks (Seattle)SNORD3G
Human Protein Atlas [tissue]ENSG00000199666-SNORD3G [tissue]
Protein Interaction databases
FunCoupENSG00000199666
BioGRIDSNORD3G
STRING (EMBL)SNORD3G
ZODIACSNORD3G
Ontologies - Pathways
Huge Navigator SNORD3G [HugePedia]
snp3D : Map Gene to Disease109616984
BioCentury BCIQSNORD3G
ClinGenSNORD3G
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD109616984
Clinical trialSNORD3G
Miscellaneous
canSAR (ICR)SNORD3G (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD3G
EVEXSNORD3G
GoPubMedSNORD3G
iHOPSNORD3G
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 13:03:06 CET 2017

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