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SNORD114-27 (small nucleolar RNA, C/D box 114-27)

Identity

Alias_symbol (synonym)14q(II-27)
Other alias
HGNC (Hugo) SNORD114-27
LocusID (NCBI) 767608
Atlas_Id 73802
Location 14q32.31  [Link to chromosome band 14q32]
Location_base_pair Starts at 100988161 and ends at 100988229 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)SNORD114-27   33015
Cards
Entrez_Gene (NCBI)SNORD114-27  767608  small nucleolar RNA, C/D box 114-27
Aliases14q(II-27)
GeneCards (Weizmann)SNORD114-27
Ensembl hg19 (Hinxton)ENSG00000200636 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000200636 [Gene_View]  chr14:100988161-100988229 [Contig_View]  SNORD114-27 [Vega]
ICGC DataPortalENSG00000200636
TCGA cBioPortalSNORD114-27
AceView (NCBI)SNORD114-27
Genatlas (Paris)SNORD114-27
WikiGenes767608
SOURCE (Princeton)SNORD114-27
Genetics Home Reference (NIH)SNORD114-27
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD114-27  -     chr14:100988161-100988229 +  14q32.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD114-27  -     14q32.31   [Description]    (hg19-Feb_2009)
EnsemblSNORD114-27 - 14q32.31 [CytoView hg19]  SNORD114-27 - 14q32.31 [CytoView hg38]
Mapping of homologs : NCBISNORD114-27 [Mapview hg19]  SNORD114-27 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD114-27
Alternative Splicing GalleryENSG00000200636
Gene ExpressionSNORD114-27 [ NCBI-GEO ]   SNORD114-27 [ EBI - ARRAY_EXPRESS ]   SNORD114-27 [ SEEK ]   SNORD114-27 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD114-27 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)767608
GTEX Portal (Tissue expression)SNORD114-27
Human Protein AtlasENSG00000200636-SNORD114-27 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD114-27
DMDM Disease mutations767608
Blocks (Seattle)SNORD114-27
Human Protein Atlas [tissue]ENSG00000200636-SNORD114-27 [tissue]
Protein Interaction databases
FunCoupENSG00000200636
BioGRIDSNORD114-27
STRING (EMBL)SNORD114-27
ZODIACSNORD114-27
Ontologies - Pathways
Huge Navigator SNORD114-27 [HugePedia]
snp3D : Map Gene to Disease767608
BioCentury BCIQSNORD114-27
ClinGenSNORD114-27
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD767608
Chemical/Pharm GKB GenePA162404199
Clinical trialSNORD114-27
Miscellaneous
canSAR (ICR)SNORD114-27 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD114-27
EVEXSNORD114-27
GoPubMedSNORD114-27
iHOPSNORD114-27
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 13:30:36 CET 2017

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