Detailed description page of humcfs

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LEPR details
Primary information
gene_nameLEPR
Humcfs IdHumcfs_617
chromosome_numberchromosome1
nameFRA1L
chrlocation61300001-84900000
cytoband1p31
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000116678
havana_transcript_idOTTHUMT00000025279
gene_location65565546-65626234
gene_orientation+
exon_idENSE00003459486, ENSE00003576938, ENSE00003547600, ENSE00003671220, ENSE00003652322, ENSE00003585777, ENSE00003575758, ENSE00003664750, ENSE00003690482, ENSE00003528068, ENSE00003683686, ENSE000012950
exon_number18
gene_descriptionleptin receptor
disease_descriptionSomatotropin deficiency,Lupus Erythematosus, Systemic,Bladder Neoplasm,Weight Loss Adverse Event,Neoplasms, Intracranial,Pregnancy in Diabetics,Obesity, Abdominal,Pituitary Neoplasms,HIV Infections,Mammary Neoplasms,Coronary heart disease,Glomerulosclerosis (disorder),Nasal Polyps,Myeloid Leukemia, Chronic,Overweight,Cardiovascular Diseases,Gestational Diabetes,Endometrial Carcinoma,Sleep Apnea, Obstructive,Precancerous Conditions,Myocardial Infarction,Weight Gain Adverse Event,Hyperphagia,Malignant tumor of colon,Amebiasis,Noninfiltrating Intraductal Carcinoma,Respiratory Tract Infections,LEPTIN RECEPTOR DEFICIENCY,Prostatic Neoplasms,Inborn Errors of Metabolism,Nephrotic Syndrome,Multiple Myeloma,Pathologic Neovascularization,Granulomatosis,Leukemia, Myelocytic, Acute,Diabetes Mellitus,Obesity,Mental disorders,Weight Gain,Albuminuria,Sleep Apnea Syndromes,Meningioma, benign, no ICD-O subtype,Tobacco Use Disorder,Colonic Neoplasms,Alzheimer Disease, Late Onset,Impaired glucose toleran
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID20198338
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