DDC

GENERAL INFORMATION

? »

Gene name

DDC

Gene description

Dopa decarboxylase (aromatic L-amino acid decarboxylase)

Protein class

Disease related genes
Enzymes
FDA approved drug targets
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

10
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Tissue enhanced (duodenum, kidney, small intestine)
GTEx:Group enriched (colon, kidney, liver, small intestine)

Protein evidence

Evidence at protein level

Protein localization

Most normal tissues displayed moderate cytoplasmic positivity. Subsets of glial cells and cells in renal tubules were strongly stained. Neuronal cells and myocytes were generally negative.

ANTIBODY RELIABILITY

? »

Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 1 antibody.
HPA017742
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Hippocampus

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Tissue enhanced (duodenum, kidney, small intestine)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (colon, kidney, liver, small intestine)

Organ

Expression



GENE INFORMATION

? »

Gene name

DDC (HGNC Symbol)

Synonyms

AADC

Description

Dopa decarboxylase (aromatic L-amino acid decarboxylase) (HGNC Symbol)

Entrez gene summary

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. [provided by RefSeq, Jun 2011]

Chromosome

7

Cytoband

Chromosome location (bp)

50458436 - 50565457

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000132437 (version 78.38)

Entrez gene

1644

UniProt

P20711 (UniProt - Evidence at protein level)

neXtProt

NX_P20711

Antibodypedia

DDC antibodies


PROTEIN BROWSER

? »
 
 
 
ENST00000357936
 
ENST00000380984
 
ENST00000420203
 
ENST00000426377
 
ENST00000430300
 
ENST00000431062
 
ENST00000444124
 
ENST00000615193
 
ENST00000617822
 
ENST00000622873
 
 
 
 


PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

DDC-001 ENSP00000350616
ENST00000357936
P20711
Show all »
Show » Show » 480 53.9 No 0
DDC-002 ENSP00000403644
ENST00000444124
P20711
Show all »
Show » Show » 480 53.9 No 0
DDC-003 ENSP00000408626
ENST00000420203
C9JMP0
Show all »
Show » 31 3.7 No 0
DDC-006 ENSP00000389422
ENST00000430300
Show » Show » 361 40.9 No 0
DDC-009 ENSP00000399184
ENST00000431062
P20711
Show all »
Show » Show » 387 44.2 No 0
DDC-013 ENSP00000395069
ENST00000426377
P20711
Show all »
Show » Show » 402 45.5 No 0
DDC-014 ENSP00000370371
ENST00000380984
P20711
Show all »
Show » Show » 338 37.1 No 0
DDC-201 ENSP00000484104
ENST00000615193
P20711
Show all »
Show » Show » 387 44.2 No 0
DDC-202 ENSP00000478385
ENST00000617822
C9JMP0
Show all »
Show » Show » 432 48.9 No 0
DDC-203 ENSP00000479110
ENST00000622873
C9JMP0
Show all »
Show » Show » 442 49.7 No 0