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SNORD14E (small nucleolar RNA, C/D box 14E)

Identity

Other alias-
HGNC (Hugo) SNORD14E
LocusID (NCBI) 85391
Atlas_Id 80047
Location 11q24.1  [Link to chromosome band 11q24]
Location_base_pair Starts at 123058077 and ends at 123058156 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)SNORD14E   30354
Cards
Entrez_Gene (NCBI)SNORD14E  85391  small nucleolar RNA, C/D box 14E
Aliases
GeneCards (Weizmann)SNORD14E
Ensembl hg19 (Hinxton)ENSG00000200879 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000200879 [Gene_View]  chr11:123058077-123058156 [Contig_View]  SNORD14E [Vega]
ICGC DataPortalENSG00000200879
TCGA cBioPortalSNORD14E
AceView (NCBI)SNORD14E
Genatlas (Paris)SNORD14E
WikiGenes85391
SOURCE (Princeton)SNORD14E
Genetics Home Reference (NIH)SNORD14E
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD14E  -     chr11:123058077-123058156 -  11q24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD14E  -     11q24.1   [Description]    (hg19-Feb_2009)
EnsemblSNORD14E - 11q24.1 [CytoView hg19]  SNORD14E - 11q24.1 [CytoView hg38]
Mapping of homologs : NCBISNORD14E [Mapview hg19]  SNORD14E [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD14E
Alternative Splicing GalleryENSG00000200879
Gene ExpressionSNORD14E [ NCBI-GEO ]   SNORD14E [ EBI - ARRAY_EXPRESS ]   SNORD14E [ SEEK ]   SNORD14E [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD14E [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)85391
GTEX Portal (Tissue expression)SNORD14E
Human Protein AtlasENSG00000200879-SNORD14E [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD14E
DMDM Disease mutations85391
Blocks (Seattle)SNORD14E
Human Protein Atlas [tissue]ENSG00000200879-SNORD14E [tissue]
Protein Interaction databases
FunCoupENSG00000200879
BioGRIDSNORD14E
STRING (EMBL)SNORD14E
ZODIACSNORD14E
Ontologies - Pathways
Huge Navigator SNORD14E [HugePedia]
snp3D : Map Gene to Disease85391
BioCentury BCIQSNORD14E
ClinGenSNORD14E
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD85391
Chemical/Pharm GKB GenePA165543686
Clinical trialSNORD14E
Miscellaneous
canSAR (ICR)SNORD14E (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD14E
EVEXSNORD14E
GoPubMedSNORD14E
iHOPSNORD14E
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 Nov 21 13:25:18 CET 2017

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