MLNR - motilin receptor Gene
Also Known as GPR38; MTLR1
Species: Homo sapiens
About MLNR
This gene has 1 transcript (splice variant), 169 orthologues and 15 paralogues. Low expression observed in reference dataset.
Summary
Motilin is a 22 amino acid peptide hormone expressed throughout the gastrointestinal (GI) tract. The protein encoded by this gene is a Motilin Receptor which is a member of the G-protein coupled receptor 1 family. This member is a multi-pass transmembrane protein, and is an important therapeutic target for the treatment of hypomotility disorders. [provided by RefSeq, Aug 2011]
MLNR Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_001507.1 | NP_001498.1 | motilin receptor |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables G protein-coupled peptide receptor activity |
IPI
IPI: Inferred from physical interaction
|
10381885 | GOA |
| enables hormone binding |
IPI
IPI: Inferred from physical interaction
|
10381885 | GOA |
MLNR Protein Structure
7tm_1: 7 transmembrane receptor (rhodopsin family) (55 - 182)
7tm_1: 7 transmembrane receptor (rhodopsin family) (233 - 355)
- 0
- 100
- 200
- 300
- 412 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
motilin receptor |
|
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Superior Mesenteric Artery Syndrome |
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| Intestinal Pseudo-Obstruction |
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| Constipation |
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| Diabetic Autonomic Neuropathy |
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| Pylorospasm |
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| Gastroparesis |
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| Benign Essential Hypertension |
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| Hypertrophic Pyloric Stenosis |
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| Functional Colonic Disease |
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| Functional Gastric Disease |
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| Rumination Disorder |
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| Lung Occult Small Cell Carcinoma |
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| Gallbladder Disease |
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| Colonic Pseudo-Obstruction |
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