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FBXO2

Gene

1 paper studies it1 finding

See all 1

C, W, M, H: cells, worms or flies, mice, humans. Dark: independent labs found the same change there. Light: one lab or one study. Outline: nothing yet.

Includes the processes named after it and trials of drugs aimed at it.

  • 1 lab in 1 country
  • Funders: National Institute on Deafness and Other Communication Disorders and 3 more
  • Humans1

Associations

1

Presbycusis

upin humans1

1 study

  1. FBXO2 is associated with presbycusis in humans.

    “Four novel ARHL genes were also detected: FBXO2 and PALM3, implicated in HL in mice, TWF1, associated with HL in Dalmatian dogs, and TXNDC17.”

    Humans

    Mendelian non-syndromic and syndromic hearing loss genes contribute to presbycusis

    European journal of human genetics : EJHG

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