SULT1C4
Sulfotransferase 1C4
Also known as: ST1C4_HUMAN, SULT1C, SULT1C2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75897
- Gene
- SULT1C4
- Ensembl
- ENSG00000198075
- Chromosome
- 2
- Canonical length
- 302 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Cytosol
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. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
302 residues, UniProt reviewed canonical sequence.
>O75897|SULT1C4
1 MALHDMEDFT FDGTKRLSVN YVKGILQPTD TCDIWDKIWN FQAKPDDLLI STYPKAGTTW
61 TQEIVELIQN EGDVEKSKRA PTHQRFPFLE MKIPSLGSGL EQAHAMPSPR ILKTHLPFHL
121 LPPSLLEKNC KIIYVARNPK DNMVSYYHFQ RMNKALPAPG TWEEYFETFL AGKVCWGSWH
181 EHVKGWWEAK DKHRILYLFY EDMKKNPKHE IQKLAEFIGK KLDDKVLDKI VHYTSFDVMK
241 QNPMANYSSI PAEIMDHSIS PFMRKGAVGD WKKHFTVAQN ERFDEDYKKK MTDTRLTFHF
301 QFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SULT1C4 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
- 29 nTPM
Expression across tissuesHPA
Tissue
- ovary: 29 nTPM
- gallbladder: 26 nTPM
- midbrain: 21 nTPM
- cervix: 21 nTPM
- basal ganglia: 19 nTPM
- hypothalamus: 18 nTPM
Single-cell type
- epididymal efferent duct ciliated cells: 81 nCPM
- cholangiocytes: 69 nCPM
- proximal tubule cells: 63 nCPM
- ependymal cells: 56 nCPM
- ovarian stromal cells: 48 nCPM
- hematopoietic stem cells: 41 nCPM
Immune cell
- basophil: 0.3 nTPM
- neutrophil: 0.1 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- midbrain: 42 nTPM
- medulla oblongata: 27 nTPM
- hypothalamus: 24 nTPM
- thalamus: 24 nTPM
- spinal cord: 22 nTPM
- pons: 21 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)
- 1.2
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.24
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
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
- 3'-phosphoadenosine 5'-phosphosulfate metabolic process
- doxorubicin metabolic process
- ethanol catabolic process
- flavonoid metabolic process
- sulfation
- xenobiotic metabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SULT1C4 as an antibody target. Whether an autoantibody or antibody against SULT1C4 could matter depends on whether native SULT1C4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SULT1C4 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 SULT1C4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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