SULT1C2
Sulfotransferase 1C2
Also known as: ST1C1, ST1C2_HUMAN, SULT1C1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O00338
- Gene
- SULT1C2
- Ensembl
- ENSG00000198203
- Chromosome
- 2
- Canonical length
- 296 aa
- Protein class
- Enzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins
OverviewNCBI Gene
Sulfotransferase enzymes catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene encodes a protein that belongs to the SULT1 subfamily, responsible for transferring a sulfo moiety from PAPS to phenol-containing compounds. Two alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
296 residues, UniProt reviewed canonical sequence.
>O00338|SULT1C2
1 MALTSDLGKQ IKLKEVEGTL LQPATVDNWS QIQSFEAKPD DLLICTYPKA GTTWIQEIVD
61 MIEQNGDVEK CQRAIIQHRH PFIEWARPPQ PSGVEKAKAM PSPRILKTHL STQLLPPSFW
121 ENNCKFLYVA RNAKDCMVSY YHFQRMNHML PDPGTWEEYF ETFINGKVVW GSWFDHVKGW
181 WEMKDRHQIL FLFYEDIKRD PKHEIRKVMQ FMGKKVDETV LDKIVQETSF EKMKENPMTN
241 RSTVSKSILD QSISSFMRKG TVGDWKNHFT VAQNERFDEI YRRKMEGTSI NFCMELLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SULT1C2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.24
- Highest tissue expression
- 154 nTPM
Expression across tissuesHPA
Tissue
- stomach: 154 nTPM
- kidney: 70 nTPM
- duodenum: 28 nTPM
- thyroid gland: 19 nTPM
- epididymis: 15 nTPM
- choroid plexus: 6.5 nTPM
Single-cell type
- foveolar cells: 934 nCPM
- distal convoluted tubule cells: 335 nCPM
- renal connecting tubule cells: 288 nCPM
- renal collecting duct intercalated cells: 261 nCPM
- proximal tubule cells: 241 nCPM
- loop of henle epithelial cells: 193 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- choroid plexus: 17 nTPM
- white matter: 3 nTPM
- thalamus: 2.1 nTPM
- pons: 2 nTPM
- hippocampal formation: 1.6 nTPM
- midbrain: 1.5 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.34
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.18
- DepMap mean gene effect
- -0.1
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SULT1C2 as an antibody target. Whether an autoantibody or antibody against SULT1C2 could matter depends on whether native SULT1C2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SULT1C2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label SULT1C2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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