abnormality of alanine metabolism Gene Set
Genes
8 genes associated with the abnormality of alanine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
CA5A
|
carbonic anhydrase VA, mitochondrial
|
|
FBXL4
|
F-box and leucine-rich repeat protein 4
|
|
MRPL3
|
mitochondrial ribosomal protein L3
|
|
MTO1
|
mitochondrial tRNA translation optimization 1
|
|
PC
|
pyruvate carboxylase
|
|
PDHA1
|
pyruvate dehydrogenase (lipoamide) alpha 1
|
|
PDHX
|
pyruvate dehydrogenase complex, component X
|
|
TMEM70
|
transmembrane protein 70
|
