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FLASH GENE
Symbol FA2H contributors: mct/shn - updated : 17-04-2013
HGNC name fatty acid 2-hydroxylase
HGNC id 21197
ASSOCIATED DISORDERS
corresponding disease(s) SDWHD , SPG35
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS
  • FA2H-siRNA in cultured human keratinocytes suppressed 2-hydroxylase activity and decreased 2-hydroxyceramide/2-hydroxyglucosylceramide levels in keratinocytes and contained abnormal epidermal lamellar bodies and did not form the normal extracellular lamellar membranes
  • FA2H-deficient (FA2H(-/-)) mice lacked 2-hydroxylated sphingolipids in the brain and in peripheral nerves while nonhydroxylated galactosylceramide is increased
  • 18-month-old FA2H(-/-) mice, however, exhibited scattered axonal and myelin sheath degeneration in the spinal cord and an even more pronounced loss of stainability of myelin sheaths in sciatic nerves