Literature summary extracted from

Remenyik, E.; Lecha, M.; Badenas, C.; Koszo, F.; Vass, V.; Herrero, C.; Varga, V.; Emri, G.; Balogh, A.; Horkay, I.
Childhood-onset mild cutaneous porphyria with compound heterozygotic mutations in the uroporphyrinogen decarboxylase gene (2008), Clin. Exp. Dermatol., 33, 602-605.

Protein Variants

EC Number	Protein Variants	Comment	Organism
4.1.1.37	M1V/P235S	the mutation is associated with UROD deficiency	Homo sapiens

Organism

EC Number	Organism	UniProt	Comment	Textmining
4.1.1.37	Homo sapiens	-	-	-

Source Tissue

EC Number	Source Tissue	Comment	Organism	Textmining
4.1.1.37	erythrocyte	-	Homo sapiens	-

Substrates and Products (Substrate)

EC Number	Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
4.1.1.37	Uroporphyrinogen III	-	Homo sapiens	Coproporphyrinogen III + 4 CO2	-	?

Synonyms

EC Number	Synonyms	Comment	Organism
4.1.1.37	UROD1	-	Homo sapiens
4.1.1.37	uroporphyrinogen decarboxylase 1	-	Homo sapiens

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Release 2023.1 (January 2023)