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SNORD112 (small nucleolar RNA, C/D box 112)

Identity

Alias_symbol (synonym)14q(0)
Other alias
HGNC (Hugo) SNORD112
LocusID (NCBI) 692215
Atlas_Id 79677
Location 14q32.2  [Link to chromosome band 14q32]
Location_base_pair Starts at 100897920 and ends at 100897996 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)SNORD112   32777
Cards
Entrez_Gene (NCBI)SNORD112  692215  small nucleolar RNA, C/D box 112
Aliases14q(0)
GeneCards (Weizmann)SNORD112
Ensembl hg19 (Hinxton)ENSG00000275662 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000275662 [Gene_View]  chr14:100897920-100897996 [Contig_View]  SNORD112 [Vega]
ICGC DataPortalENSG00000275662
TCGA cBioPortalSNORD112
AceView (NCBI)SNORD112
Genatlas (Paris)SNORD112
WikiGenes692215
SOURCE (Princeton)SNORD112
Genetics Home Reference (NIH)SNORD112
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD112  -     chr14:100897920-100897996 +  14q32.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD112  -     14q32.2   [Description]    (hg19-Feb_2009)
EnsemblSNORD112 - 14q32.2 [CytoView hg19]  SNORD112 - 14q32.2 [CytoView hg38]
Mapping of homologs : NCBISNORD112 [Mapview hg19]  SNORD112 [Mapview hg38]
OMIM613649   
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD112
Alternative Splicing GalleryENSG00000275662
Gene ExpressionSNORD112 [ NCBI-GEO ]   SNORD112 [ EBI - ARRAY_EXPRESS ]   SNORD112 [ SEEK ]   SNORD112 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD112 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)692215
GTEX Portal (Tissue expression)SNORD112
Human Protein AtlasENSG00000275662-SNORD112 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD112
DMDM Disease mutations692215
Blocks (Seattle)SNORD112
Human Protein Atlas [tissue]ENSG00000275662-SNORD112 [tissue]
Protein Interaction databases
FunCoupENSG00000275662
BioGRIDSNORD112
STRING (EMBL)SNORD112
ZODIACSNORD112
Ontologies - Pathways
Huge Navigator SNORD112 [HugePedia]
snp3D : Map Gene to Disease692215
BioCentury BCIQSNORD112
ClinGenSNORD112
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD692215
Chemical/Pharm GKB GenePA145007730
Clinical trialSNORD112
Miscellaneous
canSAR (ICR)SNORD112 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD112
EVEXSNORD112
GoPubMedSNORD112
iHOPSNORD112
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 13:30:30 CET 2017

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