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

SNORD14B (small nucleolar RNA, C/D box 14B)

Identity

Alias_namesRNU14B
RNA, U14B small nucleolar
Alias_symbol (synonym)U14B
U14
Other alias
HGNC (Hugo) SNORD14B
LocusID (NCBI) 85388
Atlas_Id 80034
Location 11p15.1  [Link to chromosome band 11p15]
Location_base_pair Starts at 17075778 and ends at 17075868 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)SNORD14B   31803
Cards
Entrez_Gene (NCBI)SNORD14B  85388  small nucleolar RNA, C/D box 14B
AliasesRNU14B; U14; U14B
GeneCards (Weizmann)SNORD14B
Ensembl hg19 (Hinxton)ENSG00000201403 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000201403 [Gene_View]  chr11:17075778-17075868 [Contig_View]  SNORD14B [Vega]
ICGC DataPortalENSG00000201403
TCGA cBioPortalSNORD14B
AceView (NCBI)SNORD14B
Genatlas (Paris)SNORD14B
WikiGenes85388
SOURCE (Princeton)SNORD14B
Genetics Home Reference (NIH)SNORD14B
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD14B  -     chr11:17075778-17075868 -  11p15.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD14B  -     11p15.1   [Description]    (hg19-Feb_2009)
EnsemblSNORD14B - 11p15.1 [CytoView hg19]  SNORD14B - 11p15.1 [CytoView hg38]
Mapping of homologs : NCBISNORD14B [Mapview hg19]  SNORD14B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD14B
Alternative Splicing GalleryENSG00000201403
Gene ExpressionSNORD14B [ NCBI-GEO ]   SNORD14B [ EBI - ARRAY_EXPRESS ]   SNORD14B [ SEEK ]   SNORD14B [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD14B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)85388
GTEX Portal (Tissue expression)SNORD14B
Human Protein AtlasENSG00000201403-SNORD14B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD14B
DMDM Disease mutations85388
Blocks (Seattle)SNORD14B
Human Protein Atlas [tissue]ENSG00000201403-SNORD14B [tissue]
Protein Interaction databases
FunCoupENSG00000201403
BioGRIDSNORD14B
STRING (EMBL)SNORD14B
ZODIACSNORD14B
Ontologies - Pathways
Huge Navigator SNORD14B [HugePedia]
snp3D : Map Gene to Disease85388
BioCentury BCIQSNORD14B
ClinGenSNORD14B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD85388
Chemical/Pharm GKB GenePA134978083
Clinical trialSNORD14B
Miscellaneous
canSAR (ICR)SNORD14B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD14B
EVEXSNORD14B
GoPubMedSNORD14B
iHOPSNORD14B
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 : Tue Nov 21 13:25:17 CET 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.