porphyria Gene Set

Dataset	GeneRIF Biological Term Annotations
Category	structural or functional annotations
Type	biological term
Description	An inherited metabolic disorder that involves certain enzymes in the heme bio-synthetic pathway resulting in the overproduction and accumulation of the porphyrins. (Human Disease Ontology, DOID_13268)
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Genes

15 genes co-occuring with the biological term porphyria in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol	Name
ALAS2	5'-aminolevulinate synthase 2
CP	ceruloplasmin (ferroxidase)
CYBRD1	cytochrome b reductase 1
CYP1A2	cytochrome P450, family 1, subfamily A, polypeptide 2
FECH	ferrochelatase
GSTM1	glutathione S-transferase mu 1
HAMP	hepcidin antimicrobial peptide
HFE	hemochromatosis
HFE2	hemochromatosis type 2 (juvenile)
HMBS	hydroxymethylbilane synthase
PPOX	protoporphyrinogen oxidase
SLC40A1	solute carrier family 40 (iron-regulated transporter), member 1
TFRC	transferrin receptor
UROD	uroporphyrinogen decarboxylase
UROS	uroporphyrinogen III synthase