SULT1C2: Sulfotransferase Family 1C Member 2

Cytosolic sulfotransferase involved in xenobiotic metabolism and hormone sulfation.

Gene Information Card

Symbol SULT1C2
Full Name Sulfotransferase Family 1C Member 2
Gene Type Protein coding
Chromosomal Location 2q12.3
NCBI Gene ID 6819 ncbi.nlm.nih.gov/gene/6819
Ensembl ID ENSG00000115970
UniProt ID O00338
OMIM ID 602386
HGNC ID 11455
Aliases ST1C2, SULT1C1, SULT1C2A

Description

SULT1C2 encodes a member of the sulfotransferase family that catalyzes the sulfate conjugation of various xenobiotics, hormones, and neurotransmitters. This cytosolic enzyme uses 3'-phosphoadenosine-5'-phosphosulfate (PAPS) as a sulfate donor. SULT1C2 is involved in the metabolism of drugs, thyroid hormones, and phenolic compounds, and is expressed in multiple tissues including liver, kidney, and gastrointestinal tract.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Hepatocellular carcinoma Altered sulfation of xenobiotics may affect detoxification and carcinogen activation; SULT1C2 expression changes observed in tumor tissues. NCBI Gene, PubMed
Thyroid hormone metabolism disorders SULT1C2 sulfates thyroid hormones, potentially modulating their activity and clearance. UniProt, OMIM

Expression Profile

Tissue Expression
Tissue nTPM level
Liver 12.5 Medium
Kidney 8.3 Medium
Small intestine 6.1 Low
Colon 4.7 Low
Stomach 3.2 Low
Cell Line Expression
Cell Line nTPM Notes
HepG2 15.0 Hepatocellular carcinoma cell line
Caco-2 7.5 Colorectal adenocarcinoma cell line
HEK293 2.1 Embryonic kidney cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.94G>A (p.Gly32Arg) Missense <0.01% Unknown functional effect; rare population variant
c.523C>T (p.Arg175Trp) Missense <0.01% Potential loss of sulfotransferase activity
Mutation functional classification

Loss of Function (LOF)

Rare missense variants may reduce enzyme activity, but no confirmed loss-of-function mutations reported in major databases.

Gain of Function (GOF)

No gain-of-function mutations documented.

Dominant Negative (DN)

No dominant-negative mutations reported.

Pathways

Sulfation of thyroid hormones (Reactome: R-HSA-209776)
Xenobiotic metabolism (KEGG: hsa00980)

Protein Summary

SULT1C2 is a 305-amino acid cytosolic sulfotransferase that catalyzes the transfer of a sulfate group from PAPS to a variety of substrates, including small phenols, thyroid hormones, and drugs. The protein is expressed in liver, kidney, and gastrointestinal tissues, and plays a role in detoxification and hormone regulation. Structural studies indicate a conserved PAPS-binding domain and substrate-binding pocket.

Related Products

Product name Cat.No. Species Gene ID
SULT1C2 Knockout HEK293 Cell Line EDJ-KQ14783 Human 6819 Details Get a Quote
SULT1C2 Knockout HCT 116 Cell Line EDJ-KQ46421 Human 6819 Details Get a Quote
SULT1C2 Knockout HeLa Cell Line EDJ-KQ54588 Human 6819 Details Get a Quote
SULT1C2 Knockout A-549 Cell Line EDJ-KQ63072 Human 6819 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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