Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

RN7SL832P (RNA, 7SL, cytoplasmic 832, pseudogene)

Identity

Other alias-
HGNC (Hugo) RN7SL832P
LocusID (NCBI) 106479524
Atlas_Id 78779
Location 2p25.1  [Link to chromosome band 2p25]
Location_base_pair Starts at 10690010 and ends at 10692095 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)RN7SL832P   46848
Cards
Entrez_Gene (NCBI)RN7SL832P  106479524  RNA, 7SL, cytoplasmic 832, pseudogene
Aliases
GeneCards (Weizmann)RN7SL832P
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr2:10690010-10692095 [Contig_View]  RN7SL832P [Vega]
TCGA cBioPortalRN7SL832P
AceView (NCBI)RN7SL832P
Genatlas (Paris)RN7SL832P
WikiGenes106479524
SOURCE (Princeton)RN7SL832P
Genetics Home Reference (NIH)RN7SL832P
Genomic and cartography
GoldenPath hg38 (UCSC)RN7SL832P  -     chr2:10690010-10692095 +  2p25.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)RN7SL832P  -     2p25.1   [Description]    (hg19-Feb_2009)
EnsemblRN7SL832P - 2p25.1 [CytoView hg19]  RN7SL832P - 2p25.1 [CytoView hg38]
Mapping of homologs : NCBIRN7SL832P [Mapview hg19]  RN7SL832P [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC036490
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)RN7SL832P
Cluster EST : UnigeneHs.646340 [ NCBI ]
CGAP (NCI)Hs.646340
Gene ExpressionRN7SL832P [ NCBI-GEO ]   RN7SL832P [ EBI - ARRAY_EXPRESS ]   RN7SL832P [ SEEK ]   RN7SL832P [ MEM ]
Gene Expression Viewer (FireBrowse)RN7SL832P [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)106479524
GTEX Portal (Tissue expression)RN7SL832P
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)RN7SL832P
DMDM Disease mutations106479524
Blocks (Seattle)RN7SL832P
Protein Interaction databases
BioGRIDRN7SL832P
STRING (EMBL)RN7SL832P
ZODIACRN7SL832P
Ontologies - Pathways
Huge Navigator RN7SL832P [HugePedia]
snp3D : Map Gene to Disease106479524
BioCentury BCIQRN7SL832P
ClinGenRN7SL832P
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD106479524
Clinical trialRN7SL832P
Miscellaneous
canSAR (ICR)RN7SL832P (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineRN7SL832P
EVEXRN7SL832P
GoPubMedRN7SL832P
iHOPRN7SL832P
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 : Tue Nov 21 13:06:12 CET 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.