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PYY3 (peptide YY 3 (pseudogene))

Identity

Alias_namespeptide YY
Alias_symbol (synonym)OTTHUMG00000021515
Other aliasPYY-III
HGNC (Hugo) PYY3
LocusID (NCBI) 644059
Atlas_Id 47478
Location Xp11.22  [Link to chromosome band Xp11]
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)PYY3   31855
Cards
Entrez_Gene (NCBI)PYY3  644059  peptide YY 3 (pseudogene)
AliasesPYY-III
GeneCards (Weizmann)PYY3
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  - [Contig_View]  PYY3 [Vega]
TCGA cBioPortalPYY3
AceView (NCBI)PYY3
Genatlas (Paris)PYY3
WikiGenes644059
SOURCE (Princeton)PYY3
Genetics Home Reference (NIH)PYY3
Genomic and cartography
GoldenPath hg38 (UCSC)PYY3  -  
GoldenPath hg19 (UCSC)PYY3  -  
EnsemblPYY3 - [CytoView hg19]  PYY3 - [CytoView hg38]
Mapping of homologs : NCBIPYY3 [Mapview hg19]  PYY3 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)NM_001109810
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)PYY3
Gene ExpressionPYY3 [ NCBI-GEO ]   PYY3 [ EBI - ARRAY_EXPRESS ]   PYY3 [ SEEK ]   PYY3 [ MEM ]
Gene Expression Viewer (FireBrowse)PYY3 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)644059
GTEX Portal (Tissue expression)PYY3
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ5JQD4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ5JQD4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ5JQD4
Splice isoforms : SwissVarQ5JQD4
PhosPhoSitePlusQ5JQD4
Domaine pattern : Prosite (Expaxy)PANCREATIC_HORMONE_2 (PS50276)   
Domains : Interpro (EBI)Pancreatic_hormone-like   
Domain families : Pfam (Sanger)Hormone_3 (PF00159)   
Domain families : Pfam (NCBI)pfam00159   
Domain families : Smart (EMBL)PAH (SM00309)  
Domain structure : Prodom (Prabi Lyon)Pancreatic_hormone-like (PD001267)   
Conserved Domain (NCBI)PYY3
DMDM Disease mutations644059
Blocks (Seattle)PYY3
SuperfamilyQ5JQD4
Peptide AtlasQ5JQD4
Protein Interaction databases
DIP (DOE-UCLA)Q5JQD4
IntAct (EBI)Q5JQD4
BioGRIDPYY3
STRING (EMBL)PYY3
ZODIACPYY3
Ontologies - Pathways
QuickGOQ5JQD4
Ontology : AmiGOG-protein coupled receptor binding  neuropeptide hormone activity  extracellular space  neuropeptide signaling pathway  cell-cell signaling  digestion  feeding behavior  regulation of appetite  
Ontology : EGO-EBIG-protein coupled receptor binding  neuropeptide hormone activity  extracellular space  neuropeptide signaling pathway  cell-cell signaling  digestion  feeding behavior  regulation of appetite  
NDEx NetworkPYY3
Atlas of Cancer Signalling NetworkPYY3
Wikipedia pathwaysPYY3
Orthology - Evolution
OrthoDB644059
Phylogenetic Trees/Animal Genes : TreeFamPYY3
HOVERGENQ5JQD4
HOGENOMQ5JQD4
Homologs : HomoloGenePYY3
Homology/Alignments : Family Browser (UCSC)PYY3
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerPYY3 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)PYY3
dbVarPYY3
ClinVarPYY3
1000_GenomesPYY3 
Exome Variant ServerPYY3
ExAC (Exome Aggregation Consortium)PYY3 (select the gene name)
Genetic variants : HAPMAP644059
Genomic Variants (DGV)PYY3 [DGVbeta]
DECIPHERPYY3 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisPYY3 
Mutations
ICGC Data PortalPYY3 
TCGA Data PortalPYY3 
Broad Tumor PortalPYY3
OASIS PortalPYY3 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICPYY3  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDPYY3
BioMutasearch PYY3
DgiDB (Drug Gene Interaction Database)PYY3
DoCM (Curated mutations)PYY3 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)PYY3 (select a term)
intoGenPYY3
Cancer3DPYY3(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenPYY3
Genetic Testing Registry PYY3
NextProtQ5JQD4 [Medical]
TSGene644059
GENETestsPYY3
Target ValidationPYY3
Huge Navigator PYY3 [HugePedia]
snp3D : Map Gene to Disease644059
BioCentury BCIQPYY3
ClinGenPYY3
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD644059
Chemical/Pharm GKB GenePA145148157
Clinical trialPYY3
Miscellaneous
canSAR (ICR)PYY3 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMinePYY3
EVEXPYY3
GoPubMedPYY3
iHOPPYY3
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Mon Sep 25 19:27:25 CEST 2017

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