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SNORD14C (small nucleolar RNA, C/D box 14C)

Identity

Other alias-
HGNC (Hugo) SNORD14C
LocusID (NCBI) 85389
Atlas_Id 79232
Location 11q24.1  [Link to chromosome band 11q24]
Location_base_pair Starts at 123059335 and ends at 123059422 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)SNORD14C   30352
Cards
Entrez_Gene (NCBI)SNORD14C  85389  small nucleolar RNA, C/D box 14C
Aliases
GeneCards (Weizmann)SNORD14C
Ensembl hg19 (Hinxton)ENSG00000202252 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000202252 [Gene_View]  chr11:123059335-123059422 [Contig_View]  SNORD14C [Vega]
ICGC DataPortalENSG00000202252
TCGA cBioPortalSNORD14C
AceView (NCBI)SNORD14C
Genatlas (Paris)SNORD14C
WikiGenes85389
SOURCE (Princeton)SNORD14C
Genetics Home Reference (NIH)SNORD14C
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD14C  -     chr11:123059335-123059422 -  11q24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD14C  -     11q24.1   [Description]    (hg19-Feb_2009)
EnsemblSNORD14C - 11q24.1 [CytoView hg19]  SNORD14C - 11q24.1 [CytoView hg38]
Mapping of homologs : NCBISNORD14C [Mapview hg19]  SNORD14C [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD14C
Alternative Splicing GalleryENSG00000202252
Gene ExpressionSNORD14C [ NCBI-GEO ]   SNORD14C [ EBI - ARRAY_EXPRESS ]   SNORD14C [ SEEK ]   SNORD14C [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD14C [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)85389
GTEX Portal (Tissue expression)SNORD14C
Human Protein AtlasENSG00000202252-SNORD14C [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD14C
DMDM Disease mutations85389
Blocks (Seattle)SNORD14C
Human Protein Atlas [tissue]ENSG00000202252-SNORD14C [tissue]
Protein Interaction databases
FunCoupENSG00000202252
BioGRIDSNORD14C
STRING (EMBL)SNORD14C
ZODIACSNORD14C
Ontologies - Pathways
Huge Navigator SNORD14C [HugePedia]
snp3D : Map Gene to Disease85389
BioCentury BCIQSNORD14C
ClinGenSNORD14C
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD85389
Chemical/Pharm GKB GenePA165543684
Clinical trialSNORD14C
Miscellaneous
canSAR (ICR)SNORD14C (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD14C
EVEXSNORD14C
GoPubMedSNORD14C
iHOPSNORD14C
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 : Tue Nov 21 13:25:18 CET 2017

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