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

SNORD77B (small nucleolar RNA, C/D box 77B)

Identity

Other alias-
HGNC (Hugo) SNORD77B
LocusID (NCBI) 109616982
Atlas_Id 79103
Location 8q22.2  [Link to chromosome band 8q22]
Location_base_pair Starts at 100004582 and ends at 100004651 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)SNORD77B   52235
Cards
Entrez_Gene (NCBI)SNORD77B  109616982  small nucleolar RNA, C/D box 77B
Aliases
GeneCards (Weizmann)SNORD77B
Ensembl hg19 (Hinxton)ENSG00000212414 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000212414 [Gene_View]  chr8:100004582-100004651 [Contig_View]  SNORD77B [Vega]
ICGC DataPortalENSG00000212414
TCGA cBioPortalSNORD77B
AceView (NCBI)SNORD77B
Genatlas (Paris)SNORD77B
WikiGenes109616982
SOURCE (Princeton)SNORD77B
Genetics Home Reference (NIH)SNORD77B
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD77B  -     chr8:100004582-100004651 +  8q22.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD77B  -     8q22.2   [Description]    (hg19-Feb_2009)
EnsemblSNORD77B - 8q22.2 [CytoView hg19]  SNORD77B - 8q22.2 [CytoView hg38]
Mapping of homologs : NCBISNORD77B [Mapview hg19]  SNORD77B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD77B
Alternative Splicing GalleryENSG00000212414
Gene ExpressionSNORD77B [ NCBI-GEO ]   SNORD77B [ EBI - ARRAY_EXPRESS ]   SNORD77B [ SEEK ]   SNORD77B [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD77B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)109616982
GTEX Portal (Tissue expression)SNORD77B
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD77B
DMDM Disease mutations109616982
Blocks (Seattle)SNORD77B
Human Protein AtlasENSG00000212414
Protein Interaction databases
FunCoupENSG00000212414
BioGRIDSNORD77B
STRING (EMBL)SNORD77B
ZODIACSNORD77B
Ontologies - Pathways
Huge Navigator SNORD77B [HugePedia]
snp3D : Map Gene to Disease109616982
BioCentury BCIQSNORD77B
ClinGenSNORD77B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD109616982
Clinical trialSNORD77B
Miscellaneous
canSAR (ICR)SNORD77B (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD77B
EVEXSNORD77B
GoPubMedSNORD77B
iHOPSNORD77B
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 13:39:56 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.