Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 57465
  • Symbol: TBC1D24
  • Description: TBC1 domain family member 24

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Disease_Term Source Rank Other Values
Deafness, autosomal dominant 65, 616044 (3) OMIM high
  • Genome region : 16p13.3
  • OMIM_ID : 613577 OMIM gene ID
  • OMIM_ID : 616044 OMIM phenotype ID
DOOR syndrome, 220500 (3) OMIM high
  • Genome region : 16p13.3
  • OMIM_ID : 220500 OMIM phenotype ID
  • OMIM_ID : 613577 OMIM gene ID
Epileptic encephalopathy, early infantile, 16, 615338 (3) OMIM high
  • Genome region : 16p13.3
  • OMIM_ID : 613577 OMIM gene ID
  • OMIM_ID : 615338 OMIM phenotype ID
Deafness , autosomal recessive 86, 614617 (3) OMIM high
  • Genome region : 16p13.3
  • OMIM_ID : 613577 OMIM gene ID
  • OMIM_ID : 614617 OMIM phenotype ID
Myoclonic epilepsy, infantile, familial, 605021 (3) OMIM high
  • Genome region : 16p13.3
  • OMIM_ID : 605021 OMIM phenotype ID
  • OMIM_ID : 613577 OMIM gene ID