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Gene Gene information from NCBI Gene database.
Entrez ID 339501
Gene name Serine protease 38
Gene symbol PRSS38
Synonyms (NCBI Gene)
MPN2
Chromosome 1
Chromosome location 1q42.13
miRNA miRNA information provided by mirtarbase database.
53 Show/Hide all (53)
miRTarBase ID miRNA Experiments Reference
MIRT646256 hsa-miR-6769a-3p HITS-CLIP 23824327
MIRT646257 hsa-miR-3127-3p HITS-CLIP 23824327
MIRT646254 hsa-miR-6756-3p HITS-CLIP 23824327
MIRT646255 hsa-miR-6892-3p HITS-CLIP 23824327
MIRT646253 hsa-miR-6832-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8 Show/Hide all (8)
GO ID Ontology Definition Evidence Reference
GO:0004252 Function Serine-type endopeptidase activity IBA
GO:0004252 Function Serine-type endopeptidase activity IEA
GO:0005576 Component Extracellular region IEA
GO:0006508 Process Proteolysis IBA
GO:0006508 Process Proteolysis IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
A1L453
Protein name Serine protease 38 (EC 3.4.21.-) (Marapsin-2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00089 Trypsin 60 → 288 Trypsin Domain
Sequence
Sequence length 326
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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 Reference Evidence Score
Cervical cancer Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Gastric cancer Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations