GRP (gastrin-releasing peptide)

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Taking over the Atlas
Dear Colleagues,
The Atlas, once more, is in great danger, and I will have to proceed to a collective economic lay-off of all the team involved in the Atlas before the begining of April 2015 (a foundation having suddenly withdrawn its commitment to support the Atlas). I ask you herein if any Scientific Society (a Society of Cytogenetics, of Clinical Genetics, of Hematology, or a Cancer Society, or any other...), any University and/or Hospital, any Charity, or any database would be interested in taking over the Atlas, in whole or in part. If taking charge of the whole lot is too big, a consortium of various actors could be the solution (I am myself trying to find partners). Could you please spread the information, contact the relevant authorities, and find partners.
Survival of the Atlas will be critically dependant upon your ability to find solutions (and urgently!).
Kind regards.
Jean-Loup Huret
Donations are also welcome

GRP (gastrin-releasing peptide)

Identity

Other names	BN
	GRP-10
	preproGRP
	proGRP
HGNC (Hugo)	GRP
LocusID (NCBI)	2922
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 DataPortal	ENSG00000134443
cBioPortal	GRP
AceView (NCBI)	GRP
Genatlas (Paris)	GRP
WikiGenes	2922
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)
Ensembl	GRP - 18q21.32 [CytoView hg19] GRP - 18q21.32 [CytoView hg38]
Mapping of homologs : NCBI	GRP [Mapview hg19] GRP [Mapview hg38]
OMIM	137260
	Gene and transcription
Genbank (Entrez)	AB102889 AK307264 BC004488 BT006803 CK903483
RefSeq transcript (Entrez)	NM_001012512 NM_001012513 NM_002091
RefSeq genomic (Entrez)	AC_000150 NC_000018 NC_018929 NT_010966 NW_001838469 NW_004929411
Consensus coding sequences : CCDS (NCBI)	GRP
Cluster EST : Unigene	Hs.153444 [ NCBI ]
CGAP (NCI)	Hs.153444
Alternative Splicing : Fast-db (Paris)	GSHG0014083
Alternative Splicing Gallery	ENSG00000134443
Gene Expression	GRP [ NCBI-GEO ] GRP [ SEEK ] GRP [ MEM ]
SOURCE (Princeton)	Expression in : [Normal Tissue Atlas] [carcinoma Classsification] [NCI60]
	Protein : pattern, domain, 3D structure
UniProt/SwissProt	P07492 (Uniprot)
NextProt	P07492 [Medical]
With graphics : InterPro	P07492
Splice isoforms : SwissVar	P07492 (Swissvar)
Domaine pattern : Prosite (Expaxy)	BOMBESIN (PS00257)
Domains : Interpro (EBI)	Bombesin Gastrin-RP
Related proteins : CluSTr	P07492
Domain families : Pfam (Sanger)	Bombesin (PF02044)
Domain families : Pfam (NCBI)	pfam02044
DMDM Disease mutations	2922
Blocks (Seattle)	P07492
Human Protein Atlas	ENSG00000134443
Peptide Atlas	P07492
HPRD	08845
IPI	IPI00011722 IPI00218671 IPI00218672 IPI00974355 IPI00980093
	Protein Interaction databases
DIP (DOE-UCLA)	P07492
IntAct (EBI)	P07492
FunCoup	ENSG00000134443
BioGRID	GRP
IntegromeDB	GRP
STRING (EMBL)	GRP
	Ontologies - Pathways
QuickGO	P07492
Ontology : AmiGO	receptor binding neuropeptide hormone activity extracellular region extracellular space signal transduction neuropeptide signaling pathway
Ontology : EGO-EBI	receptor binding neuropeptide hormone activity extracellular region extracellular space signal transduction neuropeptide signaling pathway
Protein Interaction Database	GRP
DoCM (Curated mutations)	GRP
Wikipedia pathways	GRP
	Gene fusion - rearrangements
	Polymorphisms : SNP, variants
NCBI Variation Viewer	GRP [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)	GRP
dbVar	GRP
ClinVar	GRP
1000_Genomes	GRP
Exome Variant Server	GRP
SNP (GeneSNP Utah)	GRP
SNP : HGBase	GRP
Genetic variants : HAPMAP	GRP
Genomic Variants (DGV)	GRP [DGVbeta]
	Mutations
ICGC Data Portal	ENSG00000134443
Somatic Mutations in Cancer : COSMIC	GRP
CONAN: Copy Number Analysis	GRP
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
Impact of mutations	[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor]
	Diseases
DECIPHER (Syndromes)	18:56887400-56898002
Mutations and Diseases : HGMD	GRP
OMIM	137260
Medgen	GRP
NextProt	P07492 [Medical]
GENETests	GRP
Disease Genetic Association	GRP
Huge Navigator	GRP [HugePedia] GRP [HugeCancerGEM]
snp3D : Map Gene to Disease	2922
DGIdb (Drug Gene Interaction db)	GRP
	General knowledge
Homologs : HomoloGene	GRP
Homology/Alignments : Family Browser (UCSC)	GRP
Phylogenetic Trees/Animal Genes : TreeFam	GRP
Chemical/Protein Interactions : CTD	2922
Chemical/Pharm GKB Gene	PA28999
Clinical trial	GRP
Cancer Resource (Charite)	ENSG00000134443
	Other databases
	Probes
	Litterature
PubMed	58 Pubmed reference(s) in Entrez
CoreMine	GRP
GoPubMed	GRP
iHOP	GRP

Genes in title	automatic search in PubMed
REVIEW articles	automatic search in PubMed
Last year publications	automatic search in PubMed

Search in all EBI NCBI

Contributor(s)

Written	09-2002	Dessen P, Le Minor S

Updated	12-2014	Dessen P

© Atlas of Genetics and Cytogenetics in Oncology and Haematology

indexed on : Sat Feb 14 16:06:22 CET 2015

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