Amino acid replacement: H1882Y (revision of data in FBrf0233053).
C19592468T
H1882Y | ash1-PB; H1882Y | ash1-PC
H1882Y
The mutation was originally reported as H1873W based on an outdated version of the ash1 annotation. The amino acid location of the mutation relative to the current annotation is 1882. A C to T nucleotide change in this codon leads to a H1882Y mutation.
ash1H1873W 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.
ash1H1873W is not a significant dominant suppressor of eye pigment variegation observed in the In(1)w[m4] background.
The following transheterozygotes are lethal: ash1H1873W/Df(3L)Exel9007, ash1H1873W/ash1W790term, ash1H1873W/ash1Q893term, ash1H1873W/ash1N303mut and ash1H1873W/ash1W770mut.
P{lacW}Dplac, ash1AM5 has enhancer of variegation | dominant phenotype, enhanceable by trxAM1/trx[+]
ash1AM5/ash1[+] is an enhancer of enhancer of variegation | dominant phenotype of P{lacW}Dplac, trxAM1
ash1H1873W/+, trxS2582a/+ and ash1H1873W/+, trxR1578mut/+ double heterozygotes are viable, whereas ash1H1873W/+, trxS2582b/+ double heterozygotes are semi-viable, as compared to controls.
ash1H1873W/+, trxR1578mut/+ double heterozygotes show a dominant enhancer of eye pigment variegation phenotype which is more severe than either single heterozygote.