Inferred by orthology to human genes with DO annotation (HGNC:6482)
Disease_relevance
lam-3 encodes a laminin A subunit orthologous to human laminin alpha2 (LAMA2), which when mutated leads to merosin-deficient congenital muscular dystrophy.
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.