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FLASH GENE
Symbol NIPA1 contributors: npt/mct/shn - updated : 21-10-2013
HGNC name non-imprinted in Prader-Willi/Angelman syndrome 1
HGNC id 17043
ANIMAL & CELL MODELS
  • transgenic rats expressing a human NIPA1/SPG6 mutation in neurons show marked early onset behavioral and electrophysiologic abnormalities, accumulation of tubulovesicular organelles with endosomal features that start at axonal and dendritic terminals, followed by multifocal vacuolar degeneration in both the central nervous system and peripheral nerves