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SNORD113-8 (small nucleolar RNA, C/D box 113-8)

Identity

Alias_symbol (synonym)14q(I-8)
Other alias
HGNC (Hugo) SNORD113-8
LocusID (NCBI) 767568
Atlas_Id 79607
Location 14q32.31  [Link to chromosome band 14q32]
Location_base_pair Starts at 100943451 and ends at 100943523 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)SNORD113-8   32987
Cards
Entrez_Gene (NCBI)SNORD113-8  767568  small nucleolar RNA, C/D box 113-8
Aliases14q(I-8)
GeneCards (Weizmann)SNORD113-8
Ensembl hg19 (Hinxton)ENSG00000200367 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000200367 [Gene_View]  chr14:100943451-100943523 [Contig_View]  SNORD113-8 [Vega]
ICGC DataPortalENSG00000200367
TCGA cBioPortalSNORD113-8
AceView (NCBI)SNORD113-8
Genatlas (Paris)SNORD113-8
WikiGenes767568
SOURCE (Princeton)SNORD113-8
Genetics Home Reference (NIH)SNORD113-8
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD113-8  -     chr14:100943451-100943523 +  14q32.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD113-8  -     14q32.31   [Description]    (hg19-Feb_2009)
EnsemblSNORD113-8 - 14q32.31 [CytoView hg19]  SNORD113-8 - 14q32.31 [CytoView hg38]
Mapping of homologs : NCBISNORD113-8 [Mapview hg19]  SNORD113-8 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD113-8
Alternative Splicing GalleryENSG00000200367
Gene ExpressionSNORD113-8 [ NCBI-GEO ]   SNORD113-8 [ EBI - ARRAY_EXPRESS ]   SNORD113-8 [ SEEK ]   SNORD113-8 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD113-8 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)767568
GTEX Portal (Tissue expression)SNORD113-8
Human Protein AtlasENSG00000200367-SNORD113-8 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD113-8
DMDM Disease mutations767568
Blocks (Seattle)SNORD113-8
Human Protein Atlas [tissue]ENSG00000200367-SNORD113-8 [tissue]
Protein Interaction databases
FunCoupENSG00000200367
BioGRIDSNORD113-8
STRING (EMBL)SNORD113-8
ZODIACSNORD113-8
Ontologies - Pathways
Huge Navigator SNORD113-8 [HugePedia]
snp3D : Map Gene to Disease767568
BioCentury BCIQSNORD113-8
ClinGenSNORD113-8
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD767568
Chemical/Pharm GKB GenePA162404178
Clinical trialSNORD113-8
Miscellaneous
canSAR (ICR)SNORD113-8 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD113-8
EVEXSNORD113-8
GoPubMedSNORD113-8
iHOPSNORD113-8
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Nov 21 13:30:32 CET 2017

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