Home Details
| Official Symbol of Gene | LEP |
| Species | Homo sapiens |
| Entrez Gene ID | 3952 |
| Official Full Name | leptin |
| Also known as | OB; OBS; LEPD |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000174697 MIM:164160; AllianceGenome:HGNC:6553 |
| Map Location | 7q32.1 |
| Variation Type | SNP |
| refSNP ID | rs11761556,rs2167270,rs7799039 |
| Detected Sample | N/A |
| Sample Detail | N/A |
| Detected Method | real-time PCR |
| Disease | MS |
| Disease subtype | RRMS,PPMS,SPMS,CIS |
| Population | German |
| Sample Size | 776 MS patients / 878 control subjects |
| Pubmed ID | 21664965 |
| Year | 2011 |
| Title | Polymorphisms in genes encoding leptin, ghrelin and their receptors in German multiple sclerosis patients |
| Risk Type | Disease risk |
| Main Result | Negative |
| Result | Allele and genotype frequencies did not differ significantly between MS patients and controls. |
| Mechanism/Pathway | Leptin also plays an important role in the regulation of immune responses and pro-inflammatory cytokine secretion.It binds to the leptin receptor (LEPR), which belongs to the class I cytokine receptor superfamily and acts through the classical JAK-STAT pathway. |

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