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

SNORD114-19 (small nucleolar RNA, C/D box 114-19)

Identity

Alias_symbol (synonym)14q(II-19)
Other alias
HGNC (Hugo) SNORD114-19
LocusID (NCBI) 767597
Atlas_Id 73793
Location 14q32.31  [Link to chromosome band 14q32]
Location_base_pair Starts at 100976477 and ends at 100976550 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)SNORD114-19   33007
Cards
Entrez_Gene (NCBI)SNORD114-19  767597  small nucleolar RNA, C/D box 114-19
Aliases14q(II-19)
GeneCards (Weizmann)SNORD114-19
Ensembl hg19 (Hinxton)ENSG00000199942 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000199942 [Gene_View]  chr14:100976477-100976550 [Contig_View]  SNORD114-19 [Vega]
ICGC DataPortalENSG00000199942
TCGA cBioPortalSNORD114-19
AceView (NCBI)SNORD114-19
Genatlas (Paris)SNORD114-19
WikiGenes767597
SOURCE (Princeton)SNORD114-19
Genetics Home Reference (NIH)SNORD114-19
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD114-19  -     chr14:100976477-100976550 +  14q32.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD114-19  -     14q32.31   [Description]    (hg19-Feb_2009)
EnsemblSNORD114-19 - 14q32.31 [CytoView hg19]  SNORD114-19 - 14q32.31 [CytoView hg38]
Mapping of homologs : NCBISNORD114-19 [Mapview hg19]  SNORD114-19 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD114-19
Alternative Splicing GalleryENSG00000199942
Gene ExpressionSNORD114-19 [ NCBI-GEO ]   SNORD114-19 [ EBI - ARRAY_EXPRESS ]   SNORD114-19 [ SEEK ]   SNORD114-19 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD114-19 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)767597
GTEX Portal (Tissue expression)SNORD114-19
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD114-19
DMDM Disease mutations767597
Blocks (Seattle)SNORD114-19
Human Protein AtlasENSG00000199942
Protein Interaction databases
FunCoupENSG00000199942
BioGRIDSNORD114-19
STRING (EMBL)SNORD114-19
ZODIACSNORD114-19
Ontologies - Pathways
Huge Navigator SNORD114-19 [HugePedia]
snp3D : Map Gene to Disease767597
BioCentury BCIQSNORD114-19
ClinGenSNORD114-19
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD767597
Chemical/Pharm GKB GenePA162404190
Clinical trialSNORD114-19
Miscellaneous
canSAR (ICR)SNORD114-19 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD114-19
EVEXSNORD114-19
GoPubMedSNORD114-19
iHOPSNORD114-19
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 : Fri May 19 11:55:03 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.