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RP9P (retinitis pigmentosa 9 pseudogene)

Identity

Other alias-
HGNC (Hugo) RP9P
LocusID (NCBI) 441212
Atlas_Id 72773
Location 7p14.3  [Link to chromosome band 7p14]
Location_base_pair Starts at 32916816 and ends at 32942963 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)RP9P   33969
Cards
Entrez_Gene (NCBI)RP9P  441212  retinitis pigmentosa 9 pseudogene
Aliases
GeneCards (Weizmann)RP9P
Ensembl hg19 (Hinxton)ENSG00000205763 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000205763 [Gene_View]  chr7:32916816-32942963 [Contig_View]  RP9P [Vega]
ICGC DataPortalENSG00000205763
TCGA cBioPortalRP9P
AceView (NCBI)RP9P
Genatlas (Paris)RP9P
WikiGenes441212
SOURCE (Princeton)RP9P
Genetics Home Reference (NIH)RP9P
Genomic and cartography
GoldenPath hg38 (UCSC)RP9P  -     chr7:32916816-32942963 -  7p14.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)RP9P  -     7p14.3   [Description]    (hg19-Feb_2009)
EnsemblRP9P - 7p14.3 [CytoView hg19]  RP9P - 7p14.3 [CytoView hg38]
Mapping of homologs : NCBIRP9P [Mapview hg19]  RP9P [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF274938 AK091223 BC036907 BC050570
RefSeq transcript (Entrez)NM_001039754
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)RP9P
Cluster EST : UnigeneHs.648086 [ NCBI ]
CGAP (NCI)Hs.648086
Alternative Splicing GalleryENSG00000205763
Gene ExpressionRP9P [ NCBI-GEO ]   RP9P [ EBI - ARRAY_EXPRESS ]   RP9P [ SEEK ]   RP9P [ MEM ]
Gene Expression Viewer (FireBrowse)RP9P [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)441212
GTEX Portal (Tissue expression)RP9P
Human Protein AtlasENSG00000205763-RP9P [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)RP9P
DMDM Disease mutations441212
Blocks (Seattle)RP9P
Human Protein Atlas [tissue]ENSG00000205763-RP9P [tissue]
IPIIPI00001968   
Protein Interaction databases
FunCoupENSG00000205763
BioGRIDRP9P
STRING (EMBL)RP9P
ZODIACRP9P
Ontologies - Pathways
Huge Navigator RP9P [HugePedia]
snp3D : Map Gene to Disease441212
BioCentury BCIQRP9P
ClinGenRP9P
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD441212
Clinical trialRP9P
Miscellaneous
canSAR (ICR)RP9P (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineRP9P
EVEXRP9P
GoPubMedRP9P
iHOPRP9P
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 : Thu Nov 9 12:25:35 CET 2017

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