Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   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

SNORD149 (small nucleolar RNA, C/D box 149)

Identity

Other alias-
HGNC (Hugo) SNORD149
LocusID (NCBI) 109623485
Atlas_Id 80037
Location 8q24.3  [Link to chromosome band 8q24]
Location_base_pair Starts at 143506185 and ends at 143506248 bp from pter ( according to hg38-Dec_2013)

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)SNORD149   51863
Cards
Entrez_Gene (NCBI)SNORD149  109623485  small nucleolar RNA, C/D box 149
Aliases
GeneCards (Weizmann)SNORD149
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr8:143506185-143506248 [Contig_View]  SNORD149 [Vega]
TCGA cBioPortalSNORD149
AceView (NCBI)SNORD149
Genatlas (Paris)SNORD149
WikiGenes109623485
SOURCE (Princeton)SNORD149
Genetics Home Reference (NIH)SNORD149
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD149  -     chr8:143506185-143506248 -  8q24.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD149  -     8q24.3   [Description]    (hg19-Feb_2009)
EnsemblSNORD149 - 8q24.3 [CytoView hg19]  SNORD149 - 8q24.3 [CytoView hg38]
Mapping of homologs : NCBISNORD149 [Mapview hg19]  SNORD149 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD149
Gene ExpressionSNORD149 [ NCBI-GEO ]   SNORD149 [ EBI - ARRAY_EXPRESS ]   SNORD149 [ SEEK ]   SNORD149 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD149 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)109623485
GTEX Portal (Tissue expression)SNORD149
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD149
DMDM Disease mutations109623485
Blocks (Seattle)SNORD149
Protein Interaction databases
BioGRIDSNORD149
STRING (EMBL)SNORD149
ZODIACSNORD149
Ontologies - Pathways
Huge Navigator SNORD149 [HugePedia]
snp3D : Map Gene to Disease109623485
BioCentury BCIQbiocentury.com/targets/SNORD149 TARGET=BioCentury>SNORD149
ClinGenSNORD149
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD109623485
Clinical trialSNORD149
Miscellaneous
canSAR (ICR)SNORD149 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD149
EVEXSNORD149
GoPubMedSNORD149
iHOPSNORD149
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 : Mon Sep 18 13:39:37 CEST 2017

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

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.