1. Gene
  2. CTSO - cathepsin O Gene

CTSO - cathepsin O Gene

Homo sapiens

Also known as CTSO1

Gene ID: 1519 | Gene type: protein coding

About CTSO

Cytogenetic location: 4q32.1 Genomic coordinates (GRCh38): 4:155,924,118-155,953,866 (from NCBI)

This gene has 10 transcripts (splice variants), 1 gene allele, 213 orthologues and 12 paralogues. Ubiquitous expression in gall bladder (RPKM 28.4), liver (RPKM 26.2) and 25 other tissues.

Summary

The protein encoded by the gene is a cysteine proteinase and a member of the papain superfamily. This proteolytic Enzyme is involved in cellular protein degradation and turnover. The recombinant form of this Enzyme was shown to degrade synthetic Peptides typically used as substrates for cysteine proteinases and its proteolytic activity was abolished by an inhibitor of cyteine proteinase. [provided by RefSeq, Jul 2008]

CTSO Products(1)

mRNA Protein Name
NM_001334.3 NP_001325.1 cathepsin O preproprotein
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
32814053 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

CTSO Protein Structure

Peptidase_C1

Peptidase_C1: Papain family cysteine protease (108 - 318)

  • 0
  • 100
  • 200
  • 300
  • 321 a.a.
Protein Preferred Names Protein Names

cathepsin O

CTSO Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
CTSO P43234 LMO3 Homo sapiens Q8TAP4-4 32814053
Intra
CTSO P43234 LMO3 Homo sapiens Q8TAP4-4 32814053
Intra
CTSO P43234 LMO3 Homo sapiens Q8TAP4-4 32814053
Intra
CTSO P43234 PRKCA Homo sapiens P17252 32814053
Intra
CTSO P43234 PRKCA Homo sapiens P17252 32814053
Intra
CTSO P43234 PRKCA Homo sapiens P17252 32814053
Intra
CTSO P43234 YWHAG Homo sapiens P61981 32814053
Intra
CTSO P43234 YWHAG Homo sapiens P61981 32814053
Intra
CTSO P43234 YWHAG Homo sapiens P61981 32814053
Intra
CTSO P43234 KAT5 Homo sapiens Q92993 32814053
Intra
CTSO P43234 KAT5 Homo sapiens Q92993 32814053
Intra
CTSO P43234 KAT5 Homo sapiens Q92993 32814053
Intra
CTSO P43234 SETDB1 Homo sapiens Q15047-2 32814053
Intra
CTSO P43234 SETDB1 Homo sapiens Q15047-2 32814053
Intra
CTSO P43234 SETDB1 Homo sapiens Q15047-2 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Orofaciodigital Syndrome V

OFD5

Thurston Syndrome

Orofaciodigital Syndrome 5

Polydactyly, Postaxial, With Median Cleft Of Upper Lip

Ofds V

Oral-Facial-Digital Syndrome, Type V

Orofaciodigital Syndrome, Thurston Type

Orofaciodigital Syndrome Thurston Type

Oral-Facial-Digital Syndrome 5

Polydactyly Postaxial With Median Cleft Of Upper Lip

Ofd Syndrome 5

Ofds 5

Oral Facial Digital Syndrome 5

Oral Facial Digital Syndrome Type 5

Orofaciodigital Syndrome Type 5

Oral-Facial-Digital Syndrome Type 5

Papillon-Leage And Psaume Syndrome

Orofaciodigital Syndrome, Type V

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus CTSO MGD MGI:2139628
Macaca mulatta CTSO VGNC VGNC:71561
Rattus norvegicus CTSO RGD RGD:1589156
Bos taurus CTSO VGNC VGNC:53898
Felis catus CTSO VGNC VGNC:61270
Others CTSO NCBI