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GRP (gastrin-releasing peptide)

Identity

Other namesBN
GRP-10
preproGRP
proGRP
HGNC (Hugo) GRP
LocusID (NCBI) 2922
Atlas_Id 40758
Location 18q21.32
Location_base_pair Starts at 56887400 and ends at 56898002 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)GRP   4605
Cards
Entrez_Gene (NCBI)GRP  2922  gastrin-releasing peptide
GeneCards (Weizmann)GRP
Ensembl hg19 (Hinxton)ENSG00000134443 [Gene_View]  chr18:56887400-56898002 [Contig_View]  GRP [Vega]
Ensembl hg38 (Hinxton)ENSG00000134443 [Gene_View]  chr18:56887400-56898002 [Contig_View]  GRP [Vega]
ICGC DataPortalENSG00000134443
TCGA cBioPortalGRP
AceView (NCBI)GRP
Genatlas (Paris)GRP
WikiGenes2922
SOURCE (Princeton)GRP
Genomic and cartography
GoldenPath hg19 (UCSC)GRP  -     chr18:56887400-56898002 +  18q21.32   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)GRP  -     18q21.32   [Description]    (hg38-Dec_2013)
EnsemblGRP - 18q21.32 [CytoView hg19]  GRP - 18q21.32 [CytoView hg38]
Mapping of homologs : NCBIGRP [Mapview hg19]  GRP [Mapview hg38]
OMIM137260   
Gene and transcription
Genbank (Entrez)AB102889 AK307264 BC004488 BT006803 CK903483
RefSeq transcript (Entrez)NM_001012512 NM_001012513 NM_002091
RefSeq genomic (Entrez)NC_000018 NC_018929 NT_010966 NW_004929411
Consensus coding sequences : CCDS (NCBI)GRP
Cluster EST : UnigeneHs.153444 [ NCBI ]
CGAP (NCI)Hs.153444
Alternative Splicing : Fast-db (Paris)GSHG0014083
Alternative Splicing GalleryENSG00000134443
Gene ExpressionGRP [ NCBI-GEO ]     GRP [ SEEK ]   GRP [ MEM ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)2922
Protein : pattern, domain, 3D structure
UniProt/SwissProtP07492 (Uniprot)
NextProtP07492  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP07492
Splice isoforms : SwissVarP07492 (Swissvar)
PhosPhoSitePlusP07492
Domaine pattern : Prosite (Expaxy)BOMBESIN (PS00257)   
Domains : Interpro (EBI)Bombesin    Gastrin-RP   
Domain families : Pfam (Sanger)Bombesin (PF02044)   
Domain families : Pfam (NCBI)pfam02044   
DMDM Disease mutations2922
Blocks (Seattle)GRP
Human Protein AtlasENSG00000134443
Peptide AtlasP07492
HPRD08845
IPIIPI00011722   IPI00218671   IPI00218672   IPI00974355   IPI00980093   
Protein Interaction databases
DIP (DOE-UCLA)P07492
IntAct (EBI)P07492
FunCoupENSG00000134443
BioGRIDGRP
IntegromeDBGRP
STRING (EMBL)GRP
ZODIACGRP
Ontologies - Pathways
QuickGOP07492
Ontology : AmiGOreceptor binding  neuropeptide hormone activity  extracellular region  extracellular space  signal transduction  neuropeptide signaling pathway  
Ontology : EGO-EBIreceptor binding  neuropeptide hormone activity  extracellular region  extracellular space  signal transduction  neuropeptide signaling pathway  
Protein Interaction DatabaseGRP
Atlas of Cancer Signalling NetworkGRP
Wikipedia pathwaysGRP
Orthology - Evolution
OrthoDB2922
GeneTree (enSembl)ENSG00000134443
Phylogenetic Trees/Animal Genes : TreeFamGRP
Homologs : HomoloGeneGRP
Homology/Alignments : Family Browser (UCSC)GRP
Gene fusions - Rearrangements
Polymorphisms : SNP, variants
NCBI Variation ViewerGRP [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)GRP
dbVarGRP
ClinVarGRP
1000_GenomesGRP 
Exome Variant ServerGRP
Exome Aggregation Consortium (ExAC)ENSG00000134443
SNP (GeneSNP Utah)GRP
SNP : HGBaseGRP
Genetic variants : HAPMAPGRP
Genomic Variants (DGV)GRP [DGVbeta]
Mutations
ICGC Data PortalGRP 
TCGA Data PortalGRP 
Tumor PortalGRP
TCGA Copy Number PortalGRP
Somatic Mutations in Cancer : COSMICGRP 
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch GRP
DgiDB (Drug Gene Interaction Database)GRP
DoCM (Curated mutations)GRP (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)GRP (select a term)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] 
Diseases
DECIPHER (Syndromes)18:56887400-56898002
CONAN: Copy Number AnalysisGRP 
Mutations and Diseases : HGMDGRP
OMIM137260   
MedgenGRP
NextProtP07492 [Medical]
TSGene2922
GENETestsGRP
Huge Navigator GRP [HugePedia]  GRP [HugeCancerGEM]
snp3D : Map Gene to Disease2922
BioCentury BCIQGRP
General knowledge
Chemical/Protein Interactions : CTD2922
Chemical/Pharm GKB GenePA28999
Clinical trialGRP
Other databases
Probes
Litterature
PubMed63 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGRP
GoPubMedGRP
iHOPGRP
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 : Sat Jan 16 18:44:06 CET 2016

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