Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

SNORD119 (small nucleolar RNA, C/D box 119)

Identity

Other alias-
HGNC (Hugo) SNORD119
LocusID (NCBI) 100113378
Atlas_Id 73894
Location 20p13  [Link to chromosome band 20p13]
Location_base_pair Starts at 2443598 and ends at 2443693 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)SNORD119   33558
Cards
Entrez_Gene (NCBI)SNORD119  100113378  small nucleolar RNA, C/D box 119
Aliases
GeneCards (Weizmann)SNORD119
Ensembl hg19 (Hinxton) [Gene_View]  chr20:2443598-2443693 [Contig_View]  SNORD119 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr20:2443598-2443693 [Contig_View]  SNORD119 [Vega]
TCGA cBioPortalSNORD119
AceView (NCBI)SNORD119
Genatlas (Paris)SNORD119
WikiGenes100113378
SOURCE (Princeton)SNORD119
Genetics Home Reference (NIH)SNORD119
Genomic and cartography
GoldenPath hg19 (UCSC)SNORD119  -     chr20:2443598-2443693 -  20p13   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)SNORD119  -     20p13   [Description]    (hg38-Dec_2013)
EnsemblSNORD119 - 20p13 [CytoView hg19]  SNORD119 - 20p13 [CytoView hg38]
Mapping of homologs : NCBISNORD119 [Mapview hg19]  SNORD119 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000020 NC_018931 NG_042057 NT_011387 NW_004929416
Consensus coding sequences : CCDS (NCBI)SNORD119
Gene ExpressionSNORD119 [ NCBI-GEO ]   SNORD119 [ EBI - ARRAY_EXPRESS ]   SNORD119 [ SEEK ]   SNORD119 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD119 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100113378
GTEX Portal (Tissue expression)SNORD119
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD119
DMDM Disease mutations100113378
Blocks (Seattle)SNORD119
Protein Interaction databases
BioGRIDSNORD119
STRING (EMBL)SNORD119
ZODIACSNORD119
Ontologies - Pathways
Huge Navigator SNORD119 [HugePedia]
snp3D : Map Gene to Disease100113378
BioCentury BCIQSNORD119
ClinGenSNORD119
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100113378
Chemical/Pharm GKB GenePA162404285
Clinical trialSNORD119
Miscellaneous
canSAR (ICR)SNORD119 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD119
EVEXSNORD119
GoPubMedSNORD119
iHOPSNORD119
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 Mar 14 12:45:29 CET 2017

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.