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SNORD12B (small nucleolar RNA, C/D box 12B)

Identity

Other alias-
HGNC (Hugo) SNORD12B
LocusID (NCBI) 100113393
Atlas_Id 73904
Location 20q13.13  [Link to chromosome band 20q13]
Location_base_pair Starts at 47896850 and ends at 47896952 bp from pter ( according to hg19-Feb_2009)

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)SNORD12B   33573
Cards
Entrez_Gene (NCBI)SNORD12B  100113393  small nucleolar RNA, C/D box 12B
Aliases
GeneCards (Weizmann)SNORD12B
Ensembl hg19 (Hinxton)ENSG00000222365 [Gene_View]  chr20:47896850-47896952 [Contig_View]  SNORD12B [Vega]
Ensembl hg38 (Hinxton)ENSG00000222365 [Gene_View]  chr20:47896850-47896952 [Contig_View]  SNORD12B [Vega]
ICGC DataPortalENSG00000222365
TCGA cBioPortalSNORD12B
AceView (NCBI)SNORD12B
Genatlas (Paris)SNORD12B
WikiGenes100113393
SOURCE (Princeton)SNORD12B
Genetics Home Reference (NIH)SNORD12B
Genomic and cartography
GoldenPath hg19 (UCSC)SNORD12B  -     chr20:47896850-47896952 +  20q13.13   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)SNORD12B  -     20q13.13   [Description]    (hg38-Dec_2013)
EnsemblSNORD12B - 20q13.13 [CytoView hg19]  SNORD12B - 20q13.13 [CytoView hg38]
Mapping of homologs : NCBISNORD12B [Mapview hg19]  SNORD12B [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000020 NC_018931 NT_011362 NW_004929418
Consensus coding sequences : CCDS (NCBI)SNORD12B
Cluster EST : UnigeneHs.711216 [ NCBI ]
CGAP (NCI)Hs.711216
Alternative Splicing GalleryENSG00000222365
Gene ExpressionSNORD12B [ NCBI-GEO ]   SNORD12B [ EBI - ARRAY_EXPRESS ]   SNORD12B [ SEEK ]   SNORD12B [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD12B [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100113393
GTEX Portal (Tissue expression)SNORD12B
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD12B
DMDM Disease mutations100113393
Blocks (Seattle)SNORD12B
Human Protein AtlasENSG00000222365
Protein Interaction databases
FunCoupENSG00000222365
BioGRIDSNORD12B
STRING (EMBL)SNORD12B
ZODIACSNORD12B
Ontologies - Pathways
Huge Navigator SNORD12B [HugePedia]
snp3D : Map Gene to Disease100113393
BioCentury BCIQSNORD12B
ClinGenSNORD12B
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100113393
Chemical/Pharm GKB GenePA162404294
Clinical trialSNORD12B
Miscellaneous
canSAR (ICR)SNORD12B (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD12B
EVEXSNORD12B
GoPubMedSNORD12B
iHOPSNORD12B
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 Mar 14 12:45:32 CET 2017

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