Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
25830
Gene name Gene Name - the full gene name approved by the HGNC.
Sulfotransferase family 4A member 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SULT4A1
Synonyms (NCBI Gene) Gene synonyms aliases
BR-STL-1, BRSTL1, DJ388M5.3, NST, SULTX3, hBR-STL-1
Chromosome Chromosome number
22
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q13.31
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 19439498, 21044950, 32296183
GO:0005737 Component Cytoplasm IBA 21873635
GO:0005829 Component Cytosol TAS
GO:0008146 Function Sulfotransferase activity IBA 21873635
GO:0008146 Function Sulfotransferase activity NAS 10698717
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608359 14903 ENSG00000130540
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
19125109, 16152568, 18823757, 17728668
Unknown
Disease term Disease name Evidence References Source
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 37589509
Glioblastoma Associate 33423377
Parkinson Disease Associate 32348865
Telomeric 22q13 Monosomy Syndrome Associate 30875393
Thymoma Associate 34104648