Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 84700
  • Symbol: MYO18B
  • Description: myosin XVIIIB

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Disease_Term Source Rank Other Values
Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism, 616549 (3) OMIM high
  • Genome region : 22q12.1
  • OMIM_ID : 607295 OMIM gene ID
  • OMIM_ID : 616549 OMIM phenotype ID
Mathematical ability in children with dyslexia GWAS high
Amyotrophic lateral sclerosis (sporadic) GWAS high
Schizophrenia, bipolar disorder and depression (combined) GWAS high
Copper levels GWAS high
Urate levels in lean individuals GWAS high