A curated ncRNAomics knowledgebase for bridging basic and clinical research in eye diseases.

Detail of hsa-miR-182
ncRNA name hsa-miR-182
ncRNA Category miRNA
Disease name congenital hemochromatosis with AMD
Species Homo sapiens
Tissues/Cell_line peripheral blood monolayer cells (PBMCs) and serum
Methods miRNA array, qRT-PCR, ELISA
Expression pattern up-regulated
Functional description It is overexpressed in patients with congenital hemochromatosis and AMD in comparison to AMD patients without hemochromatosis, which is involved in the posttranscriptional expression of iron-related genes: TF, TFRI, DMT1, FTL, and FPN1.
PubMed ID 28827515
Year 2017
Title MicroRNA Expression Analysis in Serum of Patients with Congenital Hemochromatosis and Age-Related Macular Degeneration (AMD).
Drug-related ncRNA NO

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