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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
surfactant protein C
Summary
- Gene Symbol
-
- SFTPC
- Aliases
-
- BRICD6
- BRICHOS domain containing 6
- PSP-C
- SMDP2
- SP-C
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Palmitate
- Proteomics identification
- Reference proteome
- Surface film
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| P11686 |
|
| A0A0S2Z4Q0 |
|
| E5RI64 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| respiratory gaseous exchange by respiratory system |
| GO Term | Evidence Code | PMID |
|---|---|---|
| alveolar lamellar body | ||
| multivesicular body lumen |
|
|
| lamellar body |
|
|
| extracellular region |
|
|
| endoplasmic reticulum membrane |
|
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:13976 | peptic esophagitis | |
| DOID:14159 | obstructive hydrocephalus | |
| DOID:14265 | pulmonary valve insufficiency | |
| DOID:1443 | cerebral degeneration | |
| DOID:14498 | lipoid proteinosis | |
| DOID:14524 | senile degeneration of brain | |
| DOID:14525 | Reye syndrome | |
| DOID:14557 | primary pulmonary hypertension | |
| DOID:1485 | cystic fibrosis | |
| DOID:1573 | communicating hydrocephalus |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002206 | Pulmonary fibrosis |
| HP:0002615 | Hypotension |
| HP:0002789 | Tachypnea |
| HP:0002875 | Exertional dyspnea |
| HP:0002878 | Respiratory failure |
| HP:0003546 | Exercise intolerance |
| HP:0005942 | Desquamative interstitial pneumonitis |
| HP:0006515 | Interstitial pneumonitis |
| HP:0006517 | Intraalveolar phospholipid accumulation |
| HP:0006519 | Alveolar cell carcinoma |
| Disease ID | Disease Name |
|---|---|
| OMIM:610913 |
|
| ORPHA:70587 |
|
| OMIM:178500 |
|
| ORPHA:2032 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 779071 | Xenbase:XB-GENE-6489007 | ||
| 108711616 | Xenbase:XB-GENE-17346349 | ||
| 100038236 | Xenbase:XB-GENE-852771 | ||
| 100087361 | ORNAN22113 | ||
| 100932570 | SARHA12224 | ||
| 100399602 | CALJA09734 | ||
| 105579236 | CERAT15411 | ||
| 707696 | MACMU43312 | ||
| 105482086 | MACNE24625 | ||
| 101023763 | PAPAN38681 |
