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

SNORD56B (small nucleolar RNA, C/D box 56B)

Identity

Alias_namesRNU56B
RNA, U56B small nuclear
Other alias
HGNC (Hugo) SNORD56B
LocusID (NCBI) 319139
Atlas_Id 73968
Location 14q24.2  [Link to chromosome band 14q24]
Location_base_pair Starts at 71398337 and ends at 71398407 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)SNORD56B   19771
Cards
Entrez_Gene (NCBI)SNORD56B  319139  small nucleolar RNA, C/D box 56B
AliasesRNU56B
GeneCards (Weizmann)SNORD56B
Ensembl hg19 (Hinxton)ENSG00000207444 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000207444 [Gene_View]  chr14:71398337-71398407 [Contig_View]  SNORD56B [Vega]
ICGC DataPortalENSG00000207444
TCGA cBioPortalSNORD56B
AceView (NCBI)SNORD56B
Genatlas (Paris)SNORD56B
WikiGenes319139
SOURCE (Princeton)SNORD56B
Genetics Home Reference (NIH)SNORD56B
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD56B  -     chr14:71398337-71398407 +  14q24.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD56B  -     14q24.2   [Description]    (hg19-Feb_2009)
EnsemblSNORD56B - 14q24.2 [CytoView hg19]  SNORD56B - 14q24.2 [CytoView hg38]
Mapping of homologs : NCBISNORD56B [Mapview hg19]  SNORD56B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD56B
Alternative Splicing GalleryENSG00000207444
Gene ExpressionSNORD56B [ NCBI-GEO ]   SNORD56B [ EBI - ARRAY_EXPRESS ]   SNORD56B [ SEEK ]   SNORD56B [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD56B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)319139
GTEX Portal (Tissue expression)SNORD56B
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD56B
DMDM Disease mutations319139
Blocks (Seattle)SNORD56B
Human Protein AtlasENSG00000207444
Protein Interaction databases
FunCoupENSG00000207444
BioGRIDSNORD56B
STRING (EMBL)SNORD56B
ZODIACSNORD56B
Ontologies - Pathways
Huge Navigator SNORD56B [HugePedia]
snp3D : Map Gene to Disease319139
BioCentury BCIQSNORD56B
ClinGenSNORD56B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD319139
Chemical/Pharm GKB GenePA162404302
Clinical trialSNORD56B
Miscellaneous
canSAR (ICR)SNORD56B (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD56B
EVEXSNORD56B
GoPubMedSNORD56B
iHOPSNORD56B
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 : Mon Sep 18 13:39:51 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.