Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity

Annotation inferences using phylogenetic trees

Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt

Gene Ontology annotation based on curation of immunofluorescence data

Combined Automated Annotation using Multiple IEA Methods

Co-inheritance of mutations in the uroporphyrinogen decarboxylase and hemochromatosis genes accelerates the onset of porphyria cutanea tarda.

Functional consequences of naturally occurring mutations in human uroporphyrinogen decarboxylase.

Description of a new mutation in hepatoerythropoietic porphyria and prenatal exclusion of a homozygous fetus.

Structural basis for tetrapyrrole coordination by uroporphyrinogen decarboxylase.

Characterization of a new mutation (R292G) and a deletion at the human uroporphyrinogen decarboxylase locus in two patients with hepatoerythropoietic porphyria.

Human uroporphyrinogen III synthase: NMR-based mapping of the active site.

Hepatoerythropoietic porphyria due to a novel mutation in the uroporphyrinogen decarboxylase gene.

A proteome-scale map of the human interactome network.

Architecture of the human interactome defines protein communities and disease networks.

Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.

A reference map of the human binary protein interactome.

Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.

UROD decarboxylates URO3 to COPRO3

UROD decarboxylates URO1 to COPRO1

UniProtKB P06132 (DCUP_HUMAN) uroporphyrinogen decarboxylase record