Detailed description page of humcfs

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SLC52A2 details
Primary information
gene_nameSLC52A2
Humcfs IdHumcfs_2387
chromosome_numberchromosome8
nameFRA8D
chrlocation139900001-146364022
cytoband8q24.3
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000185803
havana_transcript_idOTTHUMT00000382398
gene_location144354135-144359700
gene_orientation+
exon_idENSE00002188922, ENSE00001330982, ENSE00002154455
exon_number3
gene_descriptionsolute carrier family 52 (riboflavin transporter), member 2
disease_descriptionLupus Erythematosus, Systemic,Malignant neoplasm of kidney,Coronary heart disease,Spinal Cord Diseases,Endometrial Carcinoma,Arterial thrombosis,Epithelial ovarian cancer,Malignant tumor of colon,Myocarditis,Rheumatoid Arthritis,Prostatic Neoplasms,Lung diseases,Pancreatic carcinoma,Leukemia, Myelocytic, Acute,Pulmonary Emphysema,Malignant neoplasm of endometrium,Metastatic melanoma,Sepsis,Colonic Neoplasms,Cranial nerve diseases,Squamous cell carcinoma of the head and neck,Polyendocrinopathies, Autoimmune,Pancreatic Neoplasm,Prostate carcinoma,Epithelioma,Malignant neoplasm of breast,Breast Carcinoma,Tumor Angiogenesis,Mesothelioma,Renal Cell Carcinoma,Malignant Pleural Mesothelioma,Alzheimer's Disease,Turner Syndrome,Respiratory Failure,Leukemogenesis,Secondary malignant neoplasm of lymph node,Gastroesophageal reflux disease,Chronic Obstructive Airway Disease,Leishmaniasis,Proliferative vitreoretinopathy,Peutz-Jeghers Syndrome,Brown-Vialetto-Van Laere syndrome,Colon Carcinoma,Poorly
miRNA_location144079918-144079939
miRNA_strand+
miRNA_idMIMAT0027595
miRNA_namehsa-miR-6847-3p
miRNA_derived MI0022693
TechniqueFISH
PMID15381365
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