Gene Gene information from NCBI Gene database.
Entrez ID 25830
Gene name Sulfotransferase family 4A member 1
Gene symbol SULT4A1
Synonyms (NCBI Gene)
BR-STL-1BRSTL1DJ388M5.3NSTSULTX3hBR-STL-1
Chromosome 22
Chromosome location 22q13.31
Summary This gene encodes a member of the sulfotransferase family. The encoded protein is a brain-specific sulfotransferase believed to be involved in the metabolism of neurotransmitters. Polymorphisms in this gene may be associated with susceptibility to schizop
miRNA miRNA information provided by mirtarbase database.
50
miRTarBase ID miRNA Experiments Reference
MIRT1402934 hsa-miR-146a CLIP-seq
MIRT1402935 hsa-miR-146b-5p CLIP-seq
MIRT1402936 hsa-miR-298 CLIP-seq
MIRT1402937 hsa-miR-3128 CLIP-seq
MIRT1402938 hsa-miR-326 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 19439498, 21044950, 28514442, 32152050, 32296183, 32814053, 33961781
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IEA
GO:0005739 Component Mitochondrion IEA
GO:0005829 Component Cytosol IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608359 14903 ENSG00000130540
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BR01
Protein name Sulfotransferase 4A1 (ST4A1) (EC 2.8.2.-) (Brain sulfotransferase-like protein) (hBR-STL) (hBR-STL-1) (Nervous system sulfotransferase) (NST)
Protein function Atypical sulfotransferase family member with very low affinity for 3'-phospho-5'-adenylyl sulfate (PAPS) and very low catalytic activity towards L-triiodothyronine, thyroxine, estrone, p-nitrophenol, 2-naphthylamine, and 2-beta-naphthol. May hav
PDB 1ZD1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00685 Sulfotransfer_1 45 277 Sulfotransferase domain Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in the cerebral cortex and frontal lobe, slightly less in the cerebellum, occipital and temporal lobes, relatively low in the medulla and putamen, and lowest in the spinal cord. No expression detected in the pancreas (
Sequence
Sequence length 284
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Cytosolic sulfonation of small molecules
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
SCHIZOAFFECTIVE DISORDER Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Adenocarcinoma of Lung Associate 37589509
★☆☆☆☆
Found in Text Mining only
Glioblastoma Associate 33423377
★☆☆☆☆
Found in Text Mining only
Parkinson Disease Associate 32348865
★☆☆☆☆
Found in Text Mining only
Telomeric 22q13 Monosomy Syndrome Associate 30875393
★☆☆☆☆
Found in Text Mining only
Thymoma Associate 34104648
★☆☆☆☆
Found in Text Mining only