Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8460
Gene name Gene Name - the full gene name approved by the HGNC.
Tyrosylprotein sulfotransferase 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TPST1
Synonyms (NCBI Gene) Gene synonyms aliases
TANGO13A
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q11.21
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022966 hsa-miR-124-3p Microarray 18668037
MIRT2134647 hsa-miR-4496 CLIP-seq
MIRT2649389 hsa-miR-3691-3p CLIP-seq
MIRT2649390 hsa-miR-3925-5p CLIP-seq
MIRT2649391 hsa-miR-4311 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IDA 16859706
GO:0000139 Component Golgi membrane IEA
GO:0000139 Component Golgi membrane TAS
GO:0005794 Component Golgi apparatus IBA
GO:0005794 Component Golgi apparatus IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603125 12020 ENSG00000169902
Protein
UniProt ID O60507
Protein name Protein-tyrosine sulfotransferase 1 (EC 2.8.2.20) (Tyrosylprotein sulfotransferase 1) (TPST-1)
Protein function Catalyzes the O-sulfation of tyrosine residues within acidic motifs of polypeptides, using 3'-phosphoadenylyl sulfate (PAPS) as cosubstrate.
PDB 5WRI , 5WRJ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13469 Sulfotransfer_3 70 263 Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. Detected in heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. {ECO:0000269|PubMed:9501187}.
Sequence
MVGKLKQNLLLACLVISSVTVFYLGQHAMECHHRIEERSQPVKLESTRTTVRTGLDLKAN
KTFAYHKDMPLIFIGGVPRSGTTLMRAMLDAHPDIRCGEETRVIPRILALKQMWSRSSKE
KIRLDEAGVTDEVLDSAMQAFLLEIIVKHGEPAPYLCNKDPFALKSLTYLSRLFPNAKFL
LMVRDGRASVHSMISRKVTIAGFDLNSYRDCLTKWNRAIETMYNQCMEVGYKKCMLVHYE
QLVLHPERWMRTLLKFLQIPWNH
SVLHHEEMIGKAGGVSLSKVERSTDQVIKPVNVGALS
KWVGKIPPDVLQDMAVIAPMLAKLGYDPYANPPNYGKPDPKIIENTRRVYKGEFQLPDFL
KEKPQTEQVE
Sequence length 370
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Cytosolic sulfonation of small molecules
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Gout Gout N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Anti Neutrophil Cytoplasmic Antibody Associated Vasculitis Stimulate 39287711
Arthritis Rheumatoid Associate 17082220, 36969166
Asthma Associate 39893495
Calcinosis Cutis Associate 23472069
Drug Hypersensitivity Associate 39893495
Idiopathic Pulmonary Fibrosis Associate 36035368
Nasopharyngeal Carcinoma Associate 23472069
Neoplasm Metastasis Associate 23472069
Obesity Associate 39893495
Subarachnoid Hemorrhage Associate 34542421