Gene: [0Xp1123/OATL1] ornithine aminotransferase-like 1;


FAG

 A coding gene related with hyperonithinemia and retinal atrophy is located in Chr 10 (see GEM:10q26/OAT)."

REF

 PRO,LOC,FAG "Barrett DJ &: Invest Ophthal Vis Sci, 28, 1037-1041, 1987
MAP "Chand A &: Genomics, 30, 545-552, 1995
PRO,LOC,FAG "Lafreniere RG &: Genomics, 10, 276-279, 1991
LIN,MAP "Lafreniere RG &: CCG, 51, (HGM10), 1028, 1989
LIN,MAP "Mahtani &: CCG, 51, (HGM10), 1038, 1989
PRO,LOC,FAG "Mitchell &: AJHG, 39, A163, 1986
PRO,LOC,FAG "Ramesh &: Hum Genet, 76, 121-126, 1986
PRO,LOC,FAG "see also GEM:10q26/OAT

KEY

 mito, eye, neu, mtbd

CLA

 psi, basic

LOC

 0X p11.23

MIM

 MIM: 311240