SCT - secretin Gene
Species: Homo sapiens
About SCT
This gene has 1 transcript (splice variant), 1 gene allele and 54 orthologues. Biased expression in duodenum (RPKM 7.1), small intestine (RPKM 1.4) and 2 other tissues.
Summary
This gene encodes a member of the glucagon family of peptides. The encoded preproprotein is secreted by endocrine S cells in the proximal small intestinal mucosa as a prohormone, then proteolytically processed to generate the mature peptide hormone. The release of this active peptide hormone is stimulated by either fatty acids or acidic pH in the duodenum. This hormone stimulates the secretion of bile and bicarbonate in the duodenum, pancreatic and biliary ducts. [provided by RefSeq, Feb 2016]
SCT Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_021920.4 | NP_068739.1 | secretin preproprotein |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables G protein-coupled receptor binding |
IPI
IPI: Inferred from physical interaction
|
7612008 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
32296183 | GOA |
SCT Protein Structure
Hormone_2: Peptide hormone (28 - 55)
- 0
- 100
- 121 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
secretin |
|
SCT Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
SCT | P09683 | USHBP1 | Homo sapiens | Q8N6Y0 | 32296183 | |
|
Intra
|
SCT | P09683 | HOXA1 | Homo sapiens | P49639 | 32296183 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Exocrine Pancreatic Insufficiency |
|
|
| Zollinger-Ellison Syndrome |
|
|
| Pancreas Disease |
|
|
| Gastrinoma |
|
|
| Biliary Dyskinesia |
|
|
| Glucagonoma |
|
|
| Pancreatitis |
|
|
| Acute Pancreatitis |
|
|
| Duodenogastric Reflux |
|
|
| Duodenal Ulcer |
|
|
| Giardiasis |
|
|
| Peptic Ulcer Disease |
|
|
| Vipoma |
|
|
| Insulinoma |
|
|
| Duodenal Gastrinoma |
|
|
| Common Bile Duct Neoplasm |
|
|
| Multiple Endocrine Neoplasia, Type I |
|
|
| Pancreatic Gastrinoma |
|
|
| Dumping Syndrome |
|
|
| Pancreatic Cancer |
|
|
| Alcoholic Pancreatitis |
|
|
| Pancreatic Somatostatinoma |
|
|
| Gastroparesis |
|
|
| Multiple Endocrine Neoplasia |
|
|
| Pancreatic Cholera |
|
|
| Neuroendocrine Tumor |
|
|
| Hyperparathyroidism |
|
|
| Acute Hemorrhagic Pancreatitis |
|
|
| Endocrine Pancreas Disease |
|
|
| Gastritis |
|
|
| Pancreatic Steatorrhea |
|
|
| Pervasive Developmental Disorder |
|
|
| Atrophic Gastritis |
|
|
| Hypoglycemia |
|
|
| Liver Cirrhosis |
|
|
| Duodenal Atresia |
|
|
| Cystic Fibrosis |
|
|
| Duodenal Somatostatinoma |
|
|
| Autism |
|
|
| Duodenum Disease |
|
|
| Diarrhea |
|
|
| Duodenum Cancer |
|
|
| Gastric Gastrinoma |
|
|
| Pancreatitis, Hereditary |
|
|
| Diarrhea 4, Malabsorptive, Congenital |
|
|
| Primary Hyperparathyroidism |
|
|
| Cholangiocarcinoma |
|
|
| Islet Cell Tumor |
|
|
| Hyperinsulinemic Hypoglycemia, Familial, 2 |
|
|
| Autoimmune Pancreatitis |
|
|
| Dipsogenic Diabetes Insipidus |
|
|
| Cystic Kidney Disease |
|
|
| Pancreatic Cystadenoma |
|
|
| Esophageal Adenosquamous Carcinoma |
|
|
| Polymicrogyria, Bilateral Frontoparietal |
|
|
| Polycystic Liver Disease |
|
|
| Nutritional Deficiency Disease |
|
|
| Glucocorticoid Deficiency 1 |
|
|
| Inflammatory Bowel Disease |
|
|
| Diabetes Mellitus |
|
|
| Esophageal Neuroendocrine Tumor |
|
|
| Hyperinsulinemic Hypoglycemia |
|
|
| Primary Biliary Cholangitis |
|
|
| Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease |
|
|
| Schizophrenia |
|
|
| Cholangitis, Primary Sclerosing |
|
|
| Celiac Disease 1 |
|
|
| Migraine With Or Without Aura 1 |
|
|
| Type 2 Diabetes Mellitus |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Rattus norvegicus | SCT | RGD | RGD:3643 |
| Mus musculus | SCT | MGD | MGI:99466 |
| Macaca mulatta | SCT | VGNC | VGNC:107644 |
| Felis catus | SCT | VGNC | VGNC:104328 |
| Others | SCT | NCBI |