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

SNORD22 (small nucleolar RNA, C/D box 22)

Identity

Alias_namesRNU22
RNA, U22 small nucleolar
Alias_symbol (synonym)U22
Other alias
HGNC (Hugo) SNORD22
LocusID (NCBI) 9304
Atlas_Id 73923
Location 11q12.3  [Link to chromosome band 11q12]
Location_base_pair Starts at 62852910 and ends at 62853035 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)SNORD22   10145
Cards
Entrez_Gene (NCBI)SNORD22  9304  small nucleolar RNA, C/D box 22
AliasesRNU22; U22
GeneCards (Weizmann)SNORD22
Ensembl hg19 (Hinxton)ENSG00000277194 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000277194 [Gene_View]  chr11:62852910-62853035 [Contig_View]  SNORD22 [Vega]
ICGC DataPortalENSG00000277194
TCGA cBioPortalSNORD22
AceView (NCBI)SNORD22
Genatlas (Paris)SNORD22
WikiGenes9304
SOURCE (Princeton)SNORD22
Genetics Home Reference (NIH)SNORD22
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD22  -     chr11:62852910-62853035 -  11q12.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD22  -     11q12.3   [Description]    (hg19-Feb_2009)
EnsemblSNORD22 - 11q12.3 [CytoView hg19]  SNORD22 - 11q12.3 [CytoView hg38]
Mapping of homologs : NCBISNORD22 [Mapview hg19]  SNORD22 [Mapview hg38]
OMIM603223   
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD22
Cluster EST : UnigeneHs.744737 [ NCBI ]
CGAP (NCI)Hs.744737
Alternative Splicing GalleryENSG00000277194
Gene ExpressionSNORD22 [ NCBI-GEO ]   SNORD22 [ EBI - ARRAY_EXPRESS ]   SNORD22 [ SEEK ]   SNORD22 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD22 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)9304
GTEX Portal (Tissue expression)SNORD22
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD22
DMDM Disease mutations9304
Blocks (Seattle)SNORD22
Human Protein AtlasENSG00000277194
Protein Interaction databases
FunCoupENSG00000277194
BioGRIDSNORD22
STRING (EMBL)SNORD22
ZODIACSNORD22
Ontologies - Pathways
Huge Navigator SNORD22 [HugePedia]
snp3D : Map Gene to Disease9304
BioCentury BCIQSNORD22
ClinGenSNORD22
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD9304
Chemical/Pharm GKB GenePA34511
Clinical trialSNORD22
Miscellaneous
canSAR (ICR)SNORD22 (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD22
EVEXSNORD22
GoPubMedSNORD22
iHOPSNORD22
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 : Wed May 31 15:43:09 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.