PYY, peptide YY, 5697

N. diseases: 88; N. variants: 14
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1188223411
rs1188223411
Entrez Id: 5697;162417
Gene Symbol: PYY;NAGS
PYY;NAGS
CUI: C0268543
Disease:
Hyperammonemia, type III
0.710 GeneticVariation BEFREE In this study, another three families affected by NAGSD were analyzed for NAGS gene mutations resulting in the identification of three novel missense mutations (C200R [c.598T > C], S410P [c.1228T > C], A518T [c.1552G > A]). 15878741 2005
dbSNP: rs1188223411
rs1188223411
Entrez Id: 5697;162417
Gene Symbol: PYY;NAGS
PYY;NAGS
CUI: C0268543
Disease:
Hyperammonemia, type III
0.710 GeneticVariation UNIPROT
dbSNP: rs116953263
rs116953263
Entrez Id: 5697
Gene Symbol: PYY
PYY
CUI: C0005938
Disease:
Bone Density
T 0.700 GeneticVariation GWASCAT Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. 29304378 2018
dbSNP: rs760267963
rs760267963
Entrez Id: 5697;162417
Gene Symbol: PYY;NAGS
PYY;NAGS
CUI: C0268543
Disease:
Hyperammonemia, type III
0.700 GeneticVariation UNIPROT Understanding N-Acetyl-L-Glutamate Synthase Deficiency: Mutational Spectrum, Impact of Clinical Mutations on Enzyme Functionality, and Structural Considerations. 27037498 2016
dbSNP: rs760267963
rs760267963
Entrez Id: 5697;162417
Gene Symbol: PYY;NAGS
PYY;NAGS
CUI: C0268543
Disease:
Hyperammonemia, type III
0.700 GeneticVariation UNIPROT Identification of novel mutations of the human N-acetylglutamate synthase gene and their functional investigation by expression studies. 15878741 2005
dbSNP: rs760267963
rs760267963
Entrez Id: 5697;162417
Gene Symbol: PYY;NAGS
PYY;NAGS
CUI: C0268543
Disease:
Hyperammonemia, type III
0.700 GeneticVariation UNIPROT Mutation analysis in patients with N-acetylglutamate synthase deficiency. 12754705 2003
dbSNP: rs121912591
rs121912591
Entrez Id: 5697;162417
Gene Symbol: PYY;NAGS
PYY;NAGS
CUI: C0268543
Disease:
Hyperammonemia, type III
A 0.700 CausalMutation CLINVAR
dbSNP: rs1251891037
rs1251891037
Entrez Id: 5697;162417
Gene Symbol: PYY;NAGS
PYY;NAGS
CUI: C0268543
Disease:
Hyperammonemia, type III
0.700 GeneticVariation UNIPROT
dbSNP: rs1567941557
rs1567941557
Entrez Id: 5697;162417
Gene Symbol: PYY;NAGS
PYY;NAGS
CUI: C0268543
Disease:
Hyperammonemia, type III
CAGATCGGAAGA 0.700 GeneticVariation CLINVAR
dbSNP: rs755257734
rs755257734
Entrez Id: 5697;162417
Gene Symbol: PYY;NAGS
PYY;NAGS
CUI: C0268543
Disease:
Hyperammonemia, type III
A 0.700 CausalMutation CLINVAR
dbSNP: rs162431
rs162431
Entrez Id: 5697
Gene Symbol: PYY
PYY
CUI: C0524620
Disease:
Metabolic Syndrome X
0.010 GeneticVariation BEFREE A PYY haplotype extending from the proximal promoter (A-23G, rs2070592) to the 3'-UTR (C+1134A, rs162431) predicted not only plasma PYY (P = 0.009) but also other metabolic syndrome traits. 19820027 2009
dbSNP: rs2070592
rs2070592
Entrez Id: 5697
Gene Symbol: PYY
PYY
CUI: C0524620
Disease:
Metabolic Syndrome X
0.010 GeneticVariation BEFREE A PYY haplotype extending from the proximal promoter (A-23G, rs2070592) to the 3'-UTR (C+1134A, rs162431) predicted not only plasma PYY (P = 0.009) but also other metabolic syndrome traits. 19820027 2009
dbSNP: rs1258628899
rs1258628899
Entrez Id: 5697
Gene Symbol: PYY
PYY
CUI: C0020175
Disease:
Hunger
0.010 GeneticVariation BEFREE Dietary restraint and disinhibition were associated with an SNP in GHSR (477G>A, P<0.05), and perceived hunger with SNPs in GHSR and NPY (477G>A and 204T>C, P<0.05). 18957934 2008
dbSNP: rs162430
rs162430
Entrez Id: 5697
Gene Symbol: PYY
PYY
CUI: C2362324
Disease:
Pediatric Obesity
0.010 GeneticVariation BEFREE Association was also observed for an intron 3 variant (rs162430) in the PYY gene with childhood obesity (p=0.04). 17235527 2007
dbSNP: rs1058046
rs1058046
Entrez Id: 5697
Gene Symbol: PYY
PYY
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE We found no association to obesity for the PYY Arg72Thr polymorphism, which is located nearby the essential carboxy terminal. 16331299 2006
dbSNP: rs267606994
rs267606994
Entrez Id: 5697
Gene Symbol: PYY
PYY
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE A PYY Q62P variant linked to human obesity. 16368708 2006
dbSNP: rs1058046
rs1058046
Entrez Id: 5697
Gene Symbol: PYY
PYY
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE In conclusion, the common Arg allele of the PYY Arg72Thr variant modestly associates with type 2 diabetes and with type 2 diabetes-related quantitative traits. 15983231 2005
dbSNP: rs61612861
rs61612861
Entrez Id: 5697
Gene Symbol: PYY
PYY
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE Although none of these were found in 100 normal-weight white control subjects, L73P in PYY and F87I and A172T in Y2R did not segregate with obesity in family studies, and family data were unavailable for IVS2 + 32delG in PYY and L40F in Y2R. 15331560 2004