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SNORD145 (small nucleolar RNA, C/D box 145)

Identity

Other alias-
HGNC (Hugo) SNORD145
LocusID (NCBI) 109623472
Atlas_Id 79261
Location 1p34.1  [Link to chromosome band 1p34]
Location_base_pair Starts at 44670957 and ends at 44671056 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)SNORD145   51859
Cards
Entrez_Gene (NCBI)SNORD145  109623472  small nucleolar RNA, C/D box 145
Aliases
GeneCards (Weizmann)SNORD145
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr1:44670957-44671056 [Contig_View]  SNORD145 [Vega]
TCGA cBioPortalSNORD145
AceView (NCBI)SNORD145
Genatlas (Paris)SNORD145
WikiGenes109623472
SOURCE (Princeton)SNORD145
Genetics Home Reference (NIH)SNORD145
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD145  -     chr1:44670957-44671056 -  1p34.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD145  -     1p34.1   [Description]    (hg19-Feb_2009)
EnsemblSNORD145 - 1p34.1 [CytoView hg19]  SNORD145 - 1p34.1 [CytoView hg38]
Mapping of homologs : NCBISNORD145 [Mapview hg19]  SNORD145 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD145
Gene ExpressionSNORD145 [ NCBI-GEO ]   SNORD145 [ EBI - ARRAY_EXPRESS ]   SNORD145 [ SEEK ]   SNORD145 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD145 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)109623472
GTEX Portal (Tissue expression)SNORD145
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD145
DMDM Disease mutations109623472
Blocks (Seattle)SNORD145
Protein Interaction databases
BioGRIDSNORD145
STRING (EMBL)SNORD145
ZODIACSNORD145
Ontologies - Pathways
Huge Navigator SNORD145 [HugePedia]
snp3D : Map Gene to Disease109623472
BioCentury BCIQSNORD145
ClinGenSNORD145
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD109623472
Clinical trialSNORD145
Miscellaneous
canSAR (ICR)SNORD145 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD145
EVEXSNORD145
GoPubMedSNORD145
iHOPSNORD145
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 : Tue Nov 21 13:03:04 CET 2017

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