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SNORD13P1 (small nucleolar RNA, C/D box 13 pseudogene 1)

Identity

Alias_namesRNU13P1
RNA, U13 small nuclear pseudogene 1
Alias_symbol (synonym)U13
U13.32A
Other alias
HGNC (Hugo) SNORD13P1
LocusID (NCBI) 6076
Atlas_Id 79697
Location 22q13.2  [Link to chromosome band 22q13]
Location_base_pair Starts at 42076008 and ends at 42076212 bp from pter ( according to hg38-Dec_2013)
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


External links

Nomenclature
HGNC (Hugo)SNORD13P1   10110
Cards
Entrez_Gene (NCBI)SNORD13P1  6076  small nucleolar RNA, C/D box 13 pseudogene 1
AliasesRNU13P1; U13; U13.32A
GeneCards (Weizmann)SNORD13P1
Ensembl hg19 (Hinxton)ENSG00000238498 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000238498 [Gene_View]  chr22:42076008-42076212 [Contig_View]  SNORD13P1 [Vega]
ICGC DataPortalENSG00000238498
TCGA cBioPortalSNORD13P1
AceView (NCBI)SNORD13P1
Genatlas (Paris)SNORD13P1
WikiGenes6076
SOURCE (Princeton)SNORD13P1
Genetics Home Reference (NIH)SNORD13P1
Genomic and cartography
GoldenPath hg38 (UCSC)SNORD13P1  -     chr22:42076008-42076212 -  22q13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)SNORD13P1  -     22q13.2   [Description]    (hg19-Feb_2009)
EnsemblSNORD13P1 - 22q13.2 [CytoView hg19]  SNORD13P1 - 22q13.2 [CytoView hg38]
Mapping of homologs : NCBISNORD13P1 [Mapview hg19]  SNORD13P1 [Mapview hg38]
Gene and transcription
Genbank (Entrez)X58061
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)SNORD13P1
Alternative Splicing GalleryENSG00000238498
Gene ExpressionSNORD13P1 [ NCBI-GEO ]   SNORD13P1 [ EBI - ARRAY_EXPRESS ]   SNORD13P1 [ SEEK ]   SNORD13P1 [ MEM ]
Gene Expression Viewer (FireBrowse)SNORD13P1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)6076
GTEX Portal (Tissue expression)SNORD13P1
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)SNORD13P1
DMDM Disease mutations6076
Blocks (Seattle)SNORD13P1
Human Protein AtlasENSG00000238498
Protein Interaction databases
FunCoupENSG00000238498
BioGRIDSNORD13P1
STRING (EMBL)SNORD13P1
ZODIACSNORD13P1
Ontologies - Pathways
Huge Navigator SNORD13P1 [HugePedia]
snp3D : Map Gene to Disease6076
BioCentury BCIQSNORD13P1
ClinGenSNORD13P1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD6076
Chemical/Pharm GKB GenePA34475
Clinical trialSNORD13P1
Miscellaneous
canSAR (ICR)SNORD13P1 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSNORD13P1
EVEXSNORD13P1
GoPubMedSNORD13P1
iHOPSNORD13P1
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:39:35 CEST 2017

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