Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 10667
  • Symbol: FARS2
  • Description: phenylalanyl-tRNA synthetase 2, mitochondrial

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Disease_Term Source Rank Other Values
?Spastic paraplegia 77, autosomal recessive, 617046 (3) OMIM high
  • Genome region : 6p25.1
  • OMIM_ID : 611592 OMIM gene ID
  • OMIM_ID : 617046 OMIM phenotype ID
Combined oxidative phosphorylation deficiency 14, 614946 (3) OMIM high
  • Genome region : 6p25.1
  • OMIM_ID : 611592 OMIM gene ID
  • OMIM_ID : 614946 OMIM phenotype ID
Obesity (early onset extreme) GWAS high
Copper levels GWAS high