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Gene Symbol |
APLN |
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Aliases |
APEL, XNPEP2 |
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Entrez Gene ID |
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Gene Name |
Apelin |
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Chromosomal Location |
Xq26.1 |
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HGNC ID |
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Summary |
This gene encodes a peptide that functions as an endogenous ligand for the G-protein coupled apelin receptor. The encoded preproprotein is proteolytically processed into biologically active C-terminal peptide fragments. These peptide fragments activate different tissue specific signaling pathways that regulate diverse biological functions including fluid homeostasis, cardiovascular function and insulin secretion. This protein also functions as a coreceptor for the human immunodeficiency virus 1. [provided by RefSeq, Feb 2016]
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RefSeq DNA |
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RefSeq mRNA |
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e!Ensembl
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Protein Information |
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Protein Name |
Apelin, AGTRL1 ligand, APJ endogenous ligand |
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Function |
Endogenous ligand for the apelin receptor (APLNR) (PubMed:10525157). Drives internalization of the apelin receptor (By similarity). Apelin-36 dissociates more hardly than (pyroglu)apelin-13 from APLNR (By similarity). Hormone involved in the regulation of cardiac precursor cell movements during gastrulation and heart morphogenesis (By similarity). Has an inhibitory effect on cytokine production in response to T-cell receptor/CD3 cross-linking; the oral intake of apelin in the colostrum and the milk might therefore modulate immune responses in neonates (By similarity). Plays a role in early coronary blood vessels formation (By similarity). Mediates myocardial contractility in an ERK1/2-dependent manner (By similarity). May also have a role in the central control of body fluid homeostasis by influencing vasopressin release and drinking behavior (By similarity). .; (Microbial infection) Endogenous ligand for the apelin receptor (APLNR), an alternative coreceptor with CD4 for HIV-1 infection (PubMed:11090199). Inhibits HIV-1 entry in cells coexpressing CD4 and APLNR (PubMed:11090199). Apelin-36 has a greater inhibitory activity on HIV infection than other synthetic apelin derivatives (PubMed:11090199). |
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UniProt |
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Pfam |
Pfam Accession |
Pfam ID |
PF15360 |
Apelin |
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Interactions |
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STRING |
MINT |
IntAct |
ENSP00000274192 |
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P18405 |
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View interactions
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Associated Diseases
Disease group | Disease Name | References |
Cardiovascular Diseases |
Aortic Aneurysm |
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Hypertensive disease |
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Cardiovascular Abnormalities |
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Myocardial Infarction |
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Coronary heart disease |
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Pulmonary Hypertension |
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
Hyperbilirubinemia |
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Language impairment |
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Endocrine System Diseases |
PCOS |
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Diabetes Mellitus |
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Eye Diseases |
Diabetic Retinopathy |
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Musculoskeletal Diseases |
Osteoarthritis |
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Neoplasms |
Renal Cancer |
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Glioblastoma |
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Prostate cancer |
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Colorectal Cancer |
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Hematopoietic Neoplasms |
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Sarcoma |
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Liver Cancer |
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Nervous System Diseases |
Dementia |
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Nutritional and Metabolic Diseases |
Obesity |
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Metabolic Diseases |
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Hypercholesterolemia |
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Reproductive disorders |
Preeclampsia |
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References |
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PubMed ID |
Associated gene/s |
Associated condition |
Genetic Mutation |
Diagnostic Criteria |
Association with PCOS |
Ethnicity |
Conclusion |
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PCOS, obesity |
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Related
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45 women with PCOS and 45 age-matched controls |
In this study, serum apelin levels are lower in women with PCOS than in controls |
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