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SNORA35B (small nucleolar RNA, H/ACA box 35B)

Identity

Other alias-
HGNC (Hugo) SNORA35B
LocusID (NCBI) 109617004
Atlas_Id 80159
Location Xq23  [Link to chromosome band Xq23]
Location_base_pair Starts at 115126316 and ends at 115126442 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)SNORA35B   52202
Cards
Entrez_Gene (NCBI)SNORA35B  109617004  small nucleolar RNA, H/ACA box 35B
Aliases
GeneCards (Weizmann)SNORA35B
Ensembl hg19 (Hinxton)ENSG00000271907 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000271907 [Gene_View]  ENSG00000271907 [Sequence]  chrX:115126316-115126442 [Contig_View]  SNORA35B [Vega]
ICGC DataPortalENSG00000271907
TCGA cBioPortalSNORA35B
AceView (NCBI)SNORA35B
Genatlas (Paris)SNORA35B
WikiGenes109617004
SOURCE (Princeton)SNORA35B
Genetics Home Reference (NIH)SNORA35B
Genomic and cartography
GoldenPath hg38 (UCSC)SNORA35B  -     chrX:115126316-115126442 -  Xq23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORA35B  -     Xq23   [Description]    (hg19-Feb_2009)
EnsemblSNORA35B - Xq23 [CytoView hg19]  SNORA35B - Xq23 [CytoView hg38]
Mapping of homologs : NCBISNORA35B [Mapview hg19]  SNORA35B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORA35B
Alternative Splicing GalleryENSG00000271907
Gene ExpressionSNORA35B [ NCBI-GEO ]   SNORA35B [ EBI - ARRAY_EXPRESS ]   SNORA35B [ SEEK ]   SNORA35B [ MEM ]
Gene Expression Viewer (FireBrowse)SNORA35B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)109617004
GTEX Portal (Tissue expression)SNORA35B
Human Protein AtlasENSG00000271907-SNORA35B [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORA35B
DMDM Disease mutations109617004
Blocks (Seattle)SNORA35B
Human Protein Atlas [tissue]ENSG00000271907-SNORA35B [tissue]
Protein Interaction databases
FunCoupENSG00000271907
BioGRIDSNORA35B
STRING (EMBL)SNORA35B
ZODIACSNORA35B
Ontologies - Pathways
Huge Navigator SNORA35B [HugePedia]
snp3D : Map Gene to Disease109617004
BioCentury BCIQSNORA35B
ClinGenSNORA35B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD109617004
Clinical trialSNORA35B
Miscellaneous
canSAR (ICR)SNORA35B (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORA35B
EVEXSNORA35B
GoPubMedSNORA35B
iHOPSNORA35B
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Jul 30 14:30:38 CEST 2018
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