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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 |
|---|---|---|
| extracellular space | ||
| clathrin-coated endocytic vesicle |
|
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:0050156 | idiopathic pulmonary fibrosis | |
| DOID:0050158 | desquamative interstitial pneumonia | |
| DOID:0050782 | Zollinger-Ellison syndrome | |
| DOID:0050848 | obstructive sleep apnea | |
| DOID:0050997 | cerebellar ataxia, mental retardation and dysequlibrium syndrome | |
| DOID:0060185 | Clostridium difficile colitis | |
| DOID:0080348 | Alzheimer's disease 1 | |
| DOID:0090119 | ankyloblepharon-ectodermal defects-cleft lip/palate syndrome | |
| DOID:0110035 | Alzheimer's disease 2 | |
| DOID:0110037 | Alzheimer's disease 5 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0006530 | Abnormal pulmonary interstitial morphology |
| HP:0006532 | Recurrent pneumonia |
| HP:0010444 | Pulmonary insufficiency |
| HP:0010702 | Increased circulating antibody level |
| HP:0011947 | Respiratory tract infection |
| HP:0012378 | Fatigue |
| HP:0012418 | Hypoxemia |
| HP:0012735 | Cough |
| HP:0100598 | Pulmonary edema |
| HP:0100750 | Atelectasis |
| 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 |
