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SNORD19C (small nucleolar RNA, C/D box 19C)

Identity

Other alias-
HGNC (Hugo) SNORD19C
LocusID (NCBI) 109616991
Atlas_Id 80161
Location 3p21.1  [Link to chromosome band 3p21]
Location_base_pair Starts at 52691378 and ends at 52691444 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)SNORD19C   52224
Cards
Entrez_Gene (NCBI)SNORD19C  109616991  small nucleolar RNA, C/D box 19C
Aliases
GeneCards (Weizmann)SNORD19C
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chr3:52691378-52691444 [Contig_View]  SNORD19C [Vega]
TCGA cBioPortalSNORD19C
AceView (NCBI)SNORD19C
Genatlas (Paris)SNORD19C
WikiGenes109616991
SOURCE (Princeton)SNORD19C
Genetics Home Reference (NIH)SNORD19C
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD19C  -     chr3:52691378-52691444 +  3p21.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD19C  -     3p21.1   [Description]    (hg19-Feb_2009)
EnsemblSNORD19C - 3p21.1 [CytoView hg19]  SNORD19C - 3p21.1 [CytoView hg38]
Mapping of homologs : NCBISNORD19C [Mapview hg19]  SNORD19C [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD19C
Gene ExpressionSNORD19C [ NCBI-GEO ]   SNORD19C [ EBI - ARRAY_EXPRESS ]   SNORD19C [ SEEK ]   SNORD19C [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD19C [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)109616991
GTEX Portal (Tissue expression)SNORD19C
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD19C
DMDM Disease mutations109616991
Blocks (Seattle)SNORD19C
Protein Interaction databases
BioGRIDSNORD19C
STRING (EMBL)SNORD19C
ZODIACSNORD19C
Ontologies - Pathways
Huge Navigator SNORD19C [HugePedia]
snp3D : Map Gene to Disease109616991
BioCentury BCIQSNORD19C
ClinGenSNORD19C
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD109616991
Clinical trialSNORD19C
Miscellaneous
canSAR (ICR)SNORD19C (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD19C
EVEXSNORD19C
GoPubMedSNORD19C
iHOPSNORD19C
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 : Mon Jul 30 14:31:53 CEST 2018

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