malnutrition Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004395
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Genes

9 genes associated with the malnutrition phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTG2 actin, gamma 2, smooth muscle, enteric
ALDOB aldolase B, fructose-bisphosphate
COL7A1 collagen, type VII, alpha 1
COX4I2 cytochrome c oxidase subunit IV isoform 2 (lung)
MYO5B myosin VB
POLG polymerase (DNA directed), gamma
SAR1B secretion associated, Ras related GTPase 1B
SLC7A7 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
TYMP thymidine phosphorylase