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

Detail of hsa-miR-184
ncRNA name hsa-miR-184
ncRNA Category miRNA
Disease name EDICT syndrome
Species Homo sapiens
Tissues/Cell_line blood
Methods Sanger sequencing
Expression pattern associated
Functional description The single-base-pair substitution in the seed region of miR-184 is responsible for the disease phenotype observed in EDICT syndrome.
PubMed ID 22131394
Year 2012
Title A single-base substitution in the seed region of miR-184 causes EDICT syndrome.
Drug-related ncRNA NO

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