Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:25861
  • Symbol:WHRN
  • Description:whirlin

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Disease_Term Source Rank Other Values
Deafness, autosomal recessive 31, 607084 (3) OMIM high
  • Genome region :9q32
  • OMIM_ID :607084OMIM phenotype ID
  • OMIM_ID :607928OMIM gene ID
Usher syndrome, type 2D, 611383 (3) OMIM high
  • Genome region :9q32
  • OMIM_ID :607928OMIM gene ID
  • OMIM_ID :611383OMIM phenotype ID