Gene Gene information from NCBI Gene database.
Entrez ID 1521
Gene name Cathepsin W
Gene symbol CTSW
Synonyms (NCBI Gene)
LYPN
Chromosome 11
Chromosome location 11q13.1
Summary The protein encoded by this gene, a member of the peptidase C1 family, is a cysteine proteinase that may have a specific function in the mechanism or regulation of T-cell cytolytic activity. The encoded protein is found associated with the membrane inside
miRNA miRNA information provided by mirtarbase database.
1
miRTarBase ID miRNA Experiments Reference
MIRT018737 hsa-miR-335-5p Microarray 18185580
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0002376 Process Immune system process IEA
GO:0004197 Function Cysteine-type endopeptidase activity IBA
GO:0005576 Component Extracellular region TAS
GO:0005615 Component Extracellular space IBA
GO:0005737 Component Cytoplasm IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602364 2546 ENSG00000172543
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P56202
Protein name Cathepsin W (EC 3.4.22.-) (Lymphopain)
Protein function May have a specific function in the mechanism or regulation of T-cell cytolytic activity.; (Microbial infection) Plays a role during influenza virus infection in lungs cells ex vivo. Acts at the level of virus entering host cytoplasm f
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08246 Inhibitor_I29 42 99 Cathepsin propeptide inhibitor domain (I29) Domain
PF00112 Peptidase_C1 128 362 Papain family cysteine protease Domain
Tissue specificity TISSUE SPECIFICITY: Expressed predominantly in natural killer cells, and in cytotoxic T cells. {ECO:0000269|PubMed:11490002}.
Sequence
Sequence length 376
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Lysosome
Apoptosis
  Platelet degranulation
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
HYPERURICEMIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Behcet Syndrome Associate 36857067
★☆☆☆☆
Found in Text Mining only
Blood Platelet Disorders Associate 34741638
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Associate 36581948, 36835443
★☆☆☆☆
Found in Text Mining only
Carcinoma Pancreatic Ductal Associate 37794108
★☆☆☆☆
Found in Text Mining only
Celiac Disease Inhibit 16273605
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Associate 37180113
★☆☆☆☆
Found in Text Mining only
COVID 19 Associate 34741638
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Type 1 Associate 35626661
★☆☆☆☆
Found in Text Mining only
Endometrial Neoplasms Associate 30306731, 32074080
★☆☆☆☆
Found in Text Mining only
Epilepsy Inhibit 40697415
★☆☆☆☆
Found in Text Mining only