Propionic Acidemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An organic acidemia that involes a nonfunctional propionyl CoA carboxylase affecting conversion of aminio acids and fats into sugar for energy. (Human Disease Ontology, DOID_14701)
External Link https://www.disgenet.org/browser/0/1/0/C0268579
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Genes

17 genes associated with the disease Propionic Acidemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AFP alpha-fetoprotein
ARID4B AT rich interactive domain 4B (RBP1-like)
CRYGD crystallin, gamma D
GPX3 glutathione peroxidase 3
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
KCNE1 potassium channel, voltage gated subfamily E regulatory beta subunit 1
LIG4 ligase IV, DNA, ATP-dependent
MCCC2 methylcrotonoyl-CoA carboxylase 2 (beta)
MMUT methylmalonyl-CoA mutase
NAGS N-acetylglutamate synthase
OGG1 8-oxoguanine DNA glycosylase
PCCA propionyl CoA carboxylase, alpha polypeptide
PCCB propionyl CoA carboxylase, beta polypeptide
PSAT1 phosphoserine aminotransferase 1
SLC22A5 solute carrier family 22 (organic cation/carnitine transporter), member 5
TTR transthyretin
UQCRFS1 ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1