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DDC

The encoded protein catalyzes the decarboxylation of L-3,4-dihydroxyphenylalanine (DOPA) to dopamine, L-5-hydroxytryptophan to serotonin and L-tryptophan to tryptamine. Defects in this gene are the cause of aromatic L-amino-acid decarboxylase deficiency (AADCD). AADCD deficiency is an inborn error in neurotransmitter metabolism that leads to combined serotonin and catecholamine deficiency. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene.
Protein class

Disease related genes, Enzymes, FDA approved drug targets, Human disease related genes, Metabolic proteins

Predicted location

Intracellular

Single cell type specificity

Group enriched (Rod photoreceptor cells, Proximal tubular cells, Enteroendocrine cells, Proximal enterocytes)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Group enriched (CACO-2, Hep G2, OE19, SCLC-21H, SH-SY5Y)

Interaction

Homodimer.

Molecular function

Decarboxylase, Lyase

More Types Infomation

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For Research Use Only. Not For Clinical Use.

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