Gene Gene information from NCBI Gene database.
Entrez ID 203074
Gene name Serine protease 55
Gene symbol PRSS55
Synonyms (NCBI Gene)
CT153T-SP1TSP1UNQ9391
Chromosome 8
Chromosome location 8p23.1
Summary This gene encodes a member of a group of membrane-anchored chymotrypsin (S1)-like serine proteases. The enocoded protein is primarily expressed in the Leydig and Sertoli cells of the testis and may be involved in male fertility. Alternate splicing results
miRNA miRNA information provided by mirtarbase database.
9
miRTarBase ID miRNA Experiments Reference
MIRT1268611 hsa-miR-3119 CLIP-seq
MIRT1268612 hsa-miR-3150a-3p CLIP-seq
MIRT1268613 hsa-miR-3175 CLIP-seq
MIRT1268614 hsa-miR-3188 CLIP-seq
MIRT1268615 hsa-miR-4520a-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
21
GO ID Ontology Definition Evidence Reference
GO:0001669 Component Acrosomal vesicle IEA
GO:0001669 Component Acrosomal vesicle ISS
GO:0004252 Function Serine-type endopeptidase activity IEA
GO:0005737 Component Cytoplasm IEA
GO:0005829 Component Cytosol IDA 18844450
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
615144 30824 ENSG00000184647
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6UWB4
Protein name Serine protease 55 (EC 3.4.21.-) (Testis serine protease 1) (T-SP1)
Protein function Probable serine protease, which plays a crucial role in the fertility of male mice including sperm migration and sperm-egg interaction.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00089 Trypsin 68 295 Trypsin Domain
Tissue specificity TISSUE SPECIFICITY: Only detected in testis. Expressed in spermatogonia, spermatocytes, spermatids, Leydig and Sertoli cells. Expressed in prostate cancer and ovarian cancer (at protein level). {ECO:0000269|PubMed:18844450, ECO:0000269|PubMed:23436708}.
Sequence
Sequence length 352
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
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
BARRETT'S ESOPHAGUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ESOPHAGEAL ADENOCARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NEUROTIC DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OBESITY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations