1. Gene
  2. PRSS23 - serine protease 23 Gene

PRSS23 - serine protease 23 Gene

Homo sapiens

Also known as SIG13; SPUVE; ZSIG13

Gene ID: 11098 | Gene type: protein coding

About PRSS23

Cytogenetic location: 11q14.2 Genomic coordinates (GRCh38): 11:86,791,071-86,952,910 (from NCBI)

This gene has 9 transcripts (splice variants), 176 orthologues and 1 paralogue. Ubiquitous expression in gall bladder (RPKM 19.0), urinary bladder (RPKM 17.9) and 24 other tissues.

Summary

This gene encodes a conserved member of the trypsin family of serine proteases. Mouse studies found a decrease of mRNA levels of this gene after ovulation was induced. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]

PRSS23 Products(3)

mRNA Protein Name
NM_001293179.2 NP_001280108.1 serine protease 23 precursor
NM_001293180.2 NP_001280109.1 serine protease 23 precursor
NM_007173.6 NP_009104.3 serine protease 23 precursor
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 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

PRSS23 Protein Structure

Trypsin

Trypsin: Trypsin (148 - 289)

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

serine protease 23

protease, serine 23

PRSS23 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
PRSS23 O95084 SEC11C Homo sapiens Q9BY50 32296183
Intra
PRSS23 O95084 SEC11C Homo sapiens Q9BY50 32296183
Intra
PRSS23 O95084 SEC11C Homo sapiens Q9BY50 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Exudative Vitreoretinopathy 1

Retinopathy Of Prematurity

Retrolental Fibroplasia

EVR1

Criswick-Schepens Syndrome

Rop

Exudative Vitreoretinopathy, Familial, Autosomal Dominant

Fevr, Autosomal Dominant

Premature Retinopathy

Vitreoretinopathy, Exudative 1

Autosomal Dominant Familial Exudative Vitreoretinopathy

Fevr

Vitreoretinopathy, Exudative, Type 1

Retinopathy Of Prematurity Nos

Rlf- [Retrolental Fibroplasia]

Rop - [Retinopathy Of Prematurity]

Terry Syndrome

Coats Disease

Exudative Retinopathy

Retinal Telangiectasis

Coats' Disease

Leber Miliary Aneurysm

Coats' Syndrome

Congenital Retinal Telangiectasia

Exudative Vitreoretinopathy

Familial Exudative Vitreoretinopathy

Fevr

Criswick-Schepens Syndrome

Exudative Vitreoretinopathy, Familial

Vitreoretinopathy, Exudative )

Exudative Vitreoretinopathy 1

Norrie Disease

Atrophia Bulborum Hereditaria

Episkopi Blindness

Pseudoglioma

ND

Norrie-Warburg Disease

Anderson-Warburg Syndrome

Fetal Iritis Syndrome

Norrie Syndrome

Norrie-Warburg Syndrome

Ndp

Congenital Progressive Oculo-Acoustico-Cerebral Degeneration

Norrie'S Disease

Oligophrenia Microphthalmus

Pseudoglioma Congenita

Whitnall-Norman Syndrome

Fundus Dystrophy

Retinal Dystrophy

Retinal Dystrophies

Dystrophy, Retinal

Marginal Corneal Ulcer
Vascular Skin Disease

Skin Diseases, Vascular

Skin Vascular Disease

Keipert Syndrome

Nasodigitoacoustic Syndrome

KPTS

Nasodigitoacoustic Syndrome, Formerly

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
Felis catus PRSS23 VGNC VGNC:64397
Macaca mulatta PRSS23 VGNC VGNC:76253
Bos taurus PRSS23 VGNC VGNC:33416
Mus musculus PRSS23 MGD MGI:1923703
Rattus norvegicus PRSS23 RGD RGD:1359545
Canis familiaris PRSS23 VGNC VGNC:45065