PanelApp (staging)
  1. Genes and Genomic Entities
  2. MIR145

MIR145

microRNA 145
OMIM: 611795, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red MIR145 in Mendeliome


Version 1.2302

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • multisystemic smooth muscle dysfunction syndrome (MONDO:0013452), MIR145-related

Red MIR145 in Gastrointestinal neuromuscular disease


Level 2: Gastroenterological disorders
Version 1.24

Component of the following Super Panels:

  • Neuromuscular Superpanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • multisystemic smooth muscle dysfunction syndrome (MONDO:0013452)