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

Identity

Alias (NCBI)ACA29
HGNC (Hugo) SNORA29
HGNC Alias symbACA29
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)ENSG00000206910 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000206910 [Gene_View]  ENSG00000206910 [Sequence]  chr6:159785594-159785733 [Contig_View]  SNORA29 [Vega]
ICGC DataPortalENSG00000206910
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)
GoldenPathSNORA29 - 6q25.3 [CytoView hg19]  SNORA29 - 6q25.3 [CytoView hg38]
ImmunoBaseENSG00000206910
genome Data Viewer NCBISNORA29 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AJ609472
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORA29
Alternative Splicing GalleryENSG00000206910
Gene ExpressionSNORA29 [ NCBI-GEO ]   SNORA29 [ EBI - ARRAY_EXPRESS ]   SNORA29 [ SEEK ]   SNORA29 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORA29 [ Firebrowse - Broad ]
GenevisibleExpression of SNORA29 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)677812
GTEX Portal (Tissue expression)SNORA29
Human Protein AtlasENSG00000206910-SNORA29 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORA29
DMDM Disease mutations677812
Blocks (Seattle)SNORA29
Human Protein Atlas [tissue]ENSG00000206910-SNORA29 [tissue]
Protein Interaction databases
FunCoupENSG00000206910
BioGRIDSNORA29
STRING (EMBL)SNORA29
ZODIACSNORA29
Ontologies - Pathways
Huge Navigator SNORA29 [HugePedia]
snp3D : Map Gene to Disease677812
BioCentury BCIQSNORA29
ClinGenSNORA29
Clinical trials, drugs, therapy
Protein Interactions : CTD677812
Pharm GKB GenePA144596305
Clinical trialSNORA29
Miscellaneous
canSAR (ICR)SNORA29 (select the gene name)
HarmonizomeSNORA29
DataMed IndexSNORA29
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORA29
EVEXSNORA29
GoPubMedSNORA29
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Sat Aug 22 19:35:19 CEST 2020

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