Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 83636
  • Symbol: C19orf12
  • Description: chromosome 19 open reading frame 12

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Disease_Term Source Rank Other Values
?Spastic paraplegia 43, autosomal recessive, 615043 (3) OMIM high
  • Genome region : 19q12
  • OMIM_ID : 614297 OMIM gene ID
  • OMIM_ID : 615043 OMIM phenotype ID
Neurodegeneration with brain iron accumulation 4, 614298 (3) OMIM high
  • Genome region : 19q12
  • OMIM_ID : 614297 OMIM gene ID
  • OMIM_ID : 614298 OMIM phenotype ID
Response to fenofibrate (total cholesterol levels) GWAS high