loss of function allele
Splice site mutation: c592+1G>A.
G4676253A
Nucleotide substitution: GT changed to AT in the splice donor. Reported as c592+1G>A in fzr-RA.
abnormal neurophysiology | adult stage | somatic clone - tissue specific
lethal | recessive
retina | adult stage | somatic clone - tissue specific
fzrA has lethal | recessive phenotype, suppressible by Dp(1;3)DC472
fzrCR00643-TG4.2
fzrB
fzrie28
fzrunspecified
fzrG0326
Rescued by: Dp(1;3)DC120.