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10 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
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SULT1A3
sulfotransferase family 1A member 3
Chromosome 16 · 16p11.2
NCBI Gene: 6818Ensembl: ENSG00000261052.7HGNC: HGNC:11455UniProt: P0DMM9
81PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
aryl sulfotransferase activityprotein bindingsulfotransferase activitysulfate bindingneurodegenerative diseasehepatic veno-occlusive disease-immunodeficiency syndromeHepatic veno-occlusive disease - immunodeficiencyCongenital dyserythropoietic anemia type II
✦AI Summary

SULT1A3 (sulfotransferase family 1A member 3) is a cytosolic Phase II metabolic enzyme that catalyzes sulfate conjugation of catecholamine neurotransmitters and other substrates 1. The enzyme transfers a sulfonate group from 3'-phosphoadenosine 5'-phosphosulfate to endogenous compounds including dopamine, epinephrine, norepinephrine, and serotonin 2, as well as xenobiotic drugs such as phenylephrine, salbutamol, acetaminophen, and opioids 34. SULT1A3 shows high specificity for monoamine substrates, with glutamic acid at position 146 being critical for substrate recognition 5. The enzyme is abundantly expressed in intestinal tissue and specific brain regions including the superior temporal gyrus, hippocampus, and temporal lobe, where it resides in both neurons and glial cells 67. Importantly, SULT1A3 exists as a duplicated gene with SULT1A4 on chromosome 16, and multiple genetic polymorphisms affect enzyme activity 1. These polymorphisms result in differential sulfating activity toward catecholamines and therapeutic drugs, potentially impacting individual variation in drug metabolism and pharmacokinetics 342. The clinical significance of SULT1A3 polymorphisms extends to several disease associations including progressive familial intrahepatic cholestasis, Gilbert syndrome, and hemolytic anemias, though direct mechanistic links require further investigation.

Sources cited
1
SULT1A3 catalyzes sulfate conjugation of catecholamines; gene duplication of SULT1A3 and SULT1A4 on chromosome 16; identification of polymorphisms affecting enzyme activity
PMID: 15358107
2
SULT1A3 (also known as M-PST/hEST) catalyzes sulfation of steroid and phenolic substrates; alternative promoter usage generates multiple mRNA species
PMID: 8943792
3
SULT1A3 polymorphisms cause differential sulfating activity toward phenylephrine and salbutamol with variations in substrate binding affinity and catalytic activity
PMID: 31145702
4
SULT1A3/SULT1A4 polymorphisms affect sulfation of acetaminophen and opioid drugs; genetic variations impact pharmacokinetics and toxicity profiles
PMID: 29705271
5
SULT1A3 is a dopamine sulfotransferase abundantly expressed in human jejunum intestine; catalyzes sulfation of clioquinol and dopamine
PMID: 21820498
6
SULT1A3 polymorphisms cause differential sulfating activity toward catecholamines (dopamine, epinephrine, norepinephrine) and serotonin
PMID: 29524394
7
SULT1A3 has monoamine substrate specificity; glutamic acid at position 146 is critical for substrate recognition and specificity determination
PMID: 10441143
8
SULT1A3 is expressed in brain regions including superior temporal gyrus, hippocampus, and temporal lobe in both neurons and glial cells; catalyzes catecholamine metabolism
PMID: 19171676
Disease Associationsⓘ20
neurodegenerative diseaseOpen Targets
0.37Weak
Hepatic veno-occlusive disease - immunodeficiencyOpen Targets
0.04Suggestive
hepatic veno-occlusive disease-immunodeficiency syndromeOpen Targets
0.04Suggestive
congenital dyserythropoietic anemia type 2Open Targets
0.04Suggestive
Congenital dyserythropoietic anemia type IIOpen Targets
0.04Suggestive
Senior-Boichis syndromeOpen Targets
0.04Suggestive
sclerosing cholangitisOpen Targets
0.03Suggestive
hemolytic anemia due to glucophosphate isomerase deficiencyOpen Targets
0.03Suggestive
progressive familial intrahepatic cholestasis type 3Open Targets
0.03Suggestive
non-spherocytic hemolytic anemia due to hexokinase deficiencyOpen Targets
0.03Suggestive
idiopathic hypereosinophilic syndromeOpen Targets
0.03Suggestive
Crigler-Najjar syndrome type 2Open Targets
0.03Suggestive
immunodeficiency 75Open Targets
0.03Suggestive
autoinflammation with episodic fever and lymphadenopathyOpen Targets
0.03Suggestive
sickle cell diseaseOpen Targets
0.03Suggestive
cholestasis, progressive familial intrahepatic, 9Open Targets
0.03Suggestive
Hemolytic anemia due to red cell pyruvate kinase deficiencyOpen Targets
0.03Suggestive
pyruvate kinase deficiency of red cellsOpen Targets
0.03Suggestive
Gilbert syndromeOpen Targets
0.03Suggestive
immunodeficiency 118Open Targets
0.03Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
THBDProtein interaction84%GOT1Protein interaction83%SULT1C2Protein interaction71%SULT1A1Protein interaction66%SULT1A4Protein interaction60%SULT2A1Protein interaction60%
Tissue Expression6 tissues
Liver
100%
Lung
59%
Ovary
45%
Brain
22%
Bone Marrow
0%
Heart
0%
Gene Interaction Network
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SULT1A3THBDGOT1SULT1C2SULT1A1SULT1A4SULT2A1
PROTEIN STRUCTURE
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AlphaFoldAI-predicted · UniProt P0DMM9
View on AlphaFold ↗
RankingsWhere SULT1A3 stands among ~20K protein-coding genes
  • #5,905of 20,598
    Most Researched81
Genes detectedSULT1A3
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Human SULT1A3 pharmacogenetics: gene duplication and functional genomic studies.
PMID: 15358107
Biochem Biophys Res Commun · 2004
1.00
2
Steroid sulfotransferases.
PMID: 8943792
J Endocrinol · 1996
0.90
3
Impact of SULT1A3/SULT1A4 genetic polymorphisms on the sulfation of phenylephrine and salbutamol by human SULT1A3 allozymes.
PMID: 31145702
Pharmacogenet Genomics · 2019
0.80
4
Effects of human SULT1A3/SULT1A4 genetic polymorphisms on the sulfation of acetaminophen and opioid drugs by the cytosolic sulfotransferase SULT1A3.
PMID: 29705271
Arch Biochem Biophys · 2018
0.70
5
Clioquinol is sulfated by human jejunum cytosol and SULT1A3, a human-specific dopamine sulfotransferase.
PMID: 21820498
Toxicol Lett · 2011
0.60