Gene Gene information from NCBI Gene database.
Entrez ID 10279
Gene name Serine protease 16
Gene symbol PRSS16
Synonyms (NCBI Gene)
TSSP
Chromosome 6
Chromosome location 6p22.1
Summary This gene encodes a serine protease expressed exclusively in the thymus. It is thought to play a role in the alternative antigen presenting pathway used by cortical thymic epithelial cells during the positive selection of T cells. The gene is found in the
miRNA miRNA information provided by mirtarbase database.
128
miRTarBase ID miRNA Experiments Reference
MIRT030266 hsa-miR-26b-5p Microarray 19088304
MIRT570263 hsa-miR-28-5p PAR-CLIP 20371350
MIRT570262 hsa-miR-3139 PAR-CLIP 20371350
MIRT570261 hsa-miR-708-5p PAR-CLIP 20371350
MIRT570260 hsa-miR-4487 PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
15
GO ID Ontology Definition Evidence Reference
GO:0005764 Component Lysosome IBA
GO:0005764 Component Lysosome IDA 10527559
GO:0005764 Component Lysosome IEA
GO:0005768 Component Endosome IBA
GO:0005768 Component Endosome IDA 10527559
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607169 9480 ENSG00000112812
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NQE7
Protein name Thymus-specific serine protease (EC 3.4.-.-) (Serine protease 16)
Protein function Protease that may play a role in T-cell development.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05577 Peptidase_S28 64 494 Serine carboxypeptidase S28 Domain
Tissue specificity TISSUE SPECIFICITY: Expressed predominantly in cortical thymic epithelial cells.
Sequence
Sequence length 514
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
9
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTISM SPECTRUM DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GOUT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INSOMNIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Autoimmune Diseases Autoimmune Diseases BEFREE 12140752, 12144812
★☆☆☆☆
Found in Text Mining only
Autoimmune Diseases Autoimmune Diseases LHGDN 12140752
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 36204642 Associate
★☆☆☆☆
Found in Text Mining only
Celiac Disease Celiac disease BEFREE 17584581
★☆☆☆☆
Found in Text Mining only
Colitis Colitis BEFREE 25543139
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus, Insulin-Dependent Diabetes Mellitus BEFREE 12144812, 17584581, 19295542
★☆☆☆☆
Found in Text Mining only
Multiple Sclerosis Multiple Sclerosis BEFREE 29061767
★☆☆☆☆
Found in Text Mining only
Myasthenia Gravis Myasthenia Gravis BEFREE 15592422
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 25543139
★☆☆☆☆
Found in Text Mining only
Schizophrenia Schizophrenia BEFREE 22384243, 22488895
★★☆☆☆
Found in Text Mining + Unknown/Other Associations