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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
transmembrane serine protease 3
Summary
- Gene Symbol
-
- TMPRSS3
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Autocatalytic cleavage
- Disease variant
- Disulfide bond
- Endoplasmic reticulum
- Glycoprotein
- Non-syndromic deafness
- Reference proteome
- Serine protease
- Signal-anchor
- Transmembrane helix
- Zymogen
- Proteins
| UniProt | Protein Name |
|---|---|
| P57727 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| sensory perception of sound | ||
| proteolysis | ||
| intracellular sodium ion homeostasis |
| GO Term | Evidence Code | PMID |
|---|---|---|
| membrane | ||
| endoplasmic reticulum membrane | ||
| neuronal cell body | ||
| endoplasmic reticulum |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| sodium channel regulator activity | ||
| serine-type endopeptidase activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Serine protease
- Functional Category
-
- E: Amino acid transport and metabolism
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| hydrolase activity |
| proteolysis |
| serine-type endopeptidase activity |
| serine-type peptidase activity |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110527 | autosomal recessive nonsyndromic deafness 8 | |
| DOID:10003 | sensorineural hearing loss | |
| DOID:3587 | pancreatic ductal carcinoma |
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 140765 | MGI:2155445 | MOUSE22755 | ||
| 309665 | RGD:1310135 | RATNO22637 | ||
| 474016 | 9598_0:005315 | |||
| 714500 | MACMU31970 | |||
| 100000148 | ZFIN:ZDB-GENE-070912-70 | |||
| 100057972 | HORSE24777 | |||
| 100080632 | ORNAN10148 | |||
| 100171839 | 9601_0:004fa8 | PONAB21378 | ||
| 100410672 | CALJA22273 | |||
| 100490444 | Xenbase:XB-GENE-994580 |
