cutaneous porphyria Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_13271)
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Genes

21 genes co-occuring with the disease cutaneous porphyria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
UROD uroporphyrinogen decarboxylase 2.01705
UROS uroporphyrinogen III synthase 1.22172
FECH ferrochelatase 1.069
PROC protein C (inactivator of coagulation factors Va and VIIIa) 0.914727
ALAS2 5'-aminolevulinate synthase 2 0.881472
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1 0.815514
HFE2 hemochromatosis type 2 (juvenile) 0.730166
TFR2 transferrin receptor 2 0.701124
HFE hemochromatosis 0.628065
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2 0.46655
CYP2E1 cytochrome P450, family 2, subfamily E, polypeptide 1 0.400826
HAMP hepcidin antimicrobial peptide 0.358551
GSTTP1 glutathione S-transferase theta pseudogene 1 0.353763
GSTT1 glutathione S-transferase theta 1 0.353763
PPIG peptidylprolyl isomerase G (cyclophilin G) 0.334315
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1 0.332487
GSTM1 glutathione S-transferase mu 1 0.282225
GSTA3 glutathione S-transferase alpha 3 0.172799
GSTA2 glutathione S-transferase alpha 2 0.172038
GSTA4 glutathione S-transferase alpha 4 0.171286
GSTA1 glutathione S-transferase alpha 1 0.167452