abnormality of carboxylic acid metabolism Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the metabolism of a carboxylic acid. (Human Phenotype Ontology, HP_0004354)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0004354
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Genes

20 genes associated with the abnormality of carboxylic acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
MTHFR methylenetetrahydrofolate reductase (NAD(P)H) 2.58317
CPS1 carbamoyl-phosphate synthase 1, mitochondrial 1.64154
CBS cystathionine-beta-synthase 1.54733
NOX4 NADPH oxidase 4 1.42949
FANCA Fanconi anemia, complementation group A 0.856119
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase 0.808951
CUBN cubilin (intrinsic factor-cobalamin receptor) 0.733286
TRDMT1 tRNA aspartic acid methyltransferase 1 0.733286
PRDX1 peroxiredoxin 1 0.676552
FGF21 fibroblast growth factor 21 0.593319
SLC17A3 solute carrier family 17 (organic anion transporter), member 3 0.572823
GTPBP10 GTP-binding protein 10 (putative) 0.542759
GALM galactose mutarotase (aldose 1-epimerase) 0.406588
PTPRD protein tyrosine phosphatase, receptor type, D 0.405899
PLXND1 plexin D1 0.39507
LAMB1 laminin, beta 1 0.394651
ZBTB16 zinc finger and BTB domain containing 16 0.394651
LINC00320 long intergenic non-protein coding RNA 320 0.390809
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) 0.379163
KLK11 kallikrein-related peptidase 11 0.378074