Inferred by orthology to human genes with DO annotation (HGNC:8091)
Disease_relevance
C16A3.10 encodes an ornithine transaminase orthologous to the human gene OAT (ornithine aminotransferase) which when mutated leads to ornithinemia and gyrate atrophy.
Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.