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SNORA29 (small nucleolar RNA, H/ACA box 29)

Identity

Alias_symbol (synonym)ACA29
Other alias
HGNC (Hugo) SNORA29
LocusID (NCBI) 677812
Atlas_Id 73681
Location 6q25.3  [Link to chromosome band 6q25]
Location_base_pair Starts at 159785594 and ends at 159785733 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)SNORA29   32619
Cards
Entrez_Gene (NCBI)SNORA29  677812  small nucleolar RNA, H/ACA box 29
AliasesACA29
GeneCards (Weizmann)SNORA29
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chr6:159785594-159785733 [Contig_View]  SNORA29 [Vega]
TCGA cBioPortalSNORA29
AceView (NCBI)SNORA29
Genatlas (Paris)SNORA29
WikiGenes677812
SOURCE (Princeton)SNORA29
Genetics Home Reference (NIH)SNORA29
Genomic and cartography
GoldenPath hg38 (UCSC)SNORA29  -     chr6:159785594-159785733 -  6q25.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORA29  -     6q25.3   [Description]    (hg19-Feb_2009)
EnsemblSNORA29 - 6q25.3 [CytoView hg19]  SNORA29 - 6q25.3 [CytoView hg38]
Mapping of homologs : NCBISNORA29 [Mapview hg19]  SNORA29 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AJ609472
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORA29
Cluster EST : UnigeneHs.363137 [ NCBI ]
CGAP (NCI)Hs.363137
Gene ExpressionSNORA29 [ NCBI-GEO ]   SNORA29 [ EBI - ARRAY_EXPRESS ]   SNORA29 [ SEEK ]   SNORA29 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORA29 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)677812
GTEX Portal (Tissue expression)SNORA29
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORA29
DMDM Disease mutations677812
Blocks (Seattle)SNORA29
Protein Interaction databases
BioGRIDSNORA29
STRING (EMBL)SNORA29
ZODIACSNORA29
Ontologies - Pathways
Huge Navigator SNORA29 [HugePedia]
snp3D : Map Gene to Disease677812
BioCentury BCIQSNORA29
ClinGenSNORA29
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD677812
Chemical/Pharm GKB GenePA144596305
Clinical trialSNORA29
Miscellaneous
canSAR (ICR)SNORA29 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORA29
EVEXSNORA29
GoPubMedSNORA29
iHOPSNORA29
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Jul 30 14:30:36 CEST 2018

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