Amino acid replacement: Q902term (revision of data in FBrf0233053).
Amino acid replacement: Q893term.
Nucleotide substitution: C2677T.
C19595471T
Q902term | ash1-PB; Q902term | ash1-PC
Q902term
The mutation was originally reported as Q902term based on an outdated version of the ash1 annotation. The mutation relative to the current annotation is Q902term.
ash1Q893term is a dominant enhancer of eye pigment variegation observed in the E1 (combination of gypsy{}ci-E1, P{lacW}Dplac) and Pci (P{lacW}Dplac) backgrounds; no eye pigmentation silencing is observed in a P{lacW}3-76a background.
ash1Q893term is not a significant dominant suppressor of eye pigment variegation observed in the In(1)w[m4] background.
The following transheterozygotes are lethal: ash1Q893term/Df(3L)Exel9007, ash1Q893term/ash1W790term ash1Q893term/ash1N303mut, ash1Q893term/ash1H1873W and ash1Q893term/ash1W770mut.
ash1AM4, trxAM3/trx[+] has partially lethal - majority live phenotype
ash1AM4, trxAM1/trx[+] has partially lethal - majority live phenotype
ash1Q893term/+, trxS2582a/+ double heterozygotes are viable, whereas ash1Q893term/+, trxS2582b/+ and ash1Q893term/+, trxR1578mut/+ double heterozygotes are semi-viable, as compared to controls.