7bp deletion starting at nucleotide 614, causing a frameshift at amino acid 205.
Reported to be a 7bp deletion starting at nucleotide 614 causing a frame shift at aa 205; position of mutation on reference sequence inferred by FlyBase curator (using A of ATG of GB:AF044208 as position 1).
38 +/- 6.9% of ommatidia show defects in planar cell polarity in homozygotes.
Many Vangstbm-153 ommatidia over- or under-rotate; the variance (s.d.) in degree of rotation is greater than in wild type in adult eyes.
Homozygotes show defects in ommatidial polarity.
20% of Vangstbm-153 homozygous embryos fail to hatch, exhibiting a phenotype similar to unfertilized eggs. 81% of Vangstbm-7-6/Vangstbm-153 embryos fail to hatch, exhibiting a phenotype similar to unfertilized eggs. Approximately 23% of Vangstbm-7-6/Vangstbm-153 embryos are capable of reaching the 2-5 hour stage of development.
Homozygotes exhibit a range of polarity defects in the eye. 39.8% of ommatidia show polarity defects.
Vangstbm-153 has abnormal planar polarity phenotype, enhanceable by scrib[+]/scrib673
Vangstbm-153 has abnormal planar polarity phenotype, enhanceable by scrib[+]/scrib1
Vangstbm-153 has abnormal planar polarity phenotype, enhanceable by bdg164/bdg164
Vangstbm-153 has abnormal planar polarity phenotype, enhanceable by stanfrz3
Vangstbm-153 has abnormal planar polarity phenotype, enhanceable by pk1
Vangstbm-153 is an enhancer of abnormal planar polarity phenotype of stanfrz3
Vangstbm-153/Vang[+] is a non-enhancer of visible | adult stage phenotype of Nab2EP3716, Scer\GAL4GMR.PU
Vangstbm-153/Vang[+] is a non-enhancer of decreased size | adult stage phenotype of Nab2EP3716, Scer\GAL4GMR.PU
Vangstbm-153/Vang[+] is a non-suppressor of visible | adult stage phenotype of Nab2EP3716, Scer\GAL4GMR.PU
Vangstbm-153/Vang[+] is a non-suppressor of decreased size | adult stage phenotype of Nab2EP3716, Scer\GAL4GMR.PU
Vangstbm-153 has ommatidium phenotype, enhanceable by scrib[+]/scrib673
Vangstbm-153 has ommatidium phenotype, enhanceable by scrib[+]/scrib1
Vangstbm-153 has ommatidium phenotype, enhanceable by bdg164/bdg164
Vangstbm-153 has ommatidium phenotype, enhanceable by stanfrz3
Vangstbm-153 has ommatidium phenotype, enhanceable by pk1
Vangstbm-153 has ommatidium phenotype, non-enhanceable by dlg1[+]/dlg114
Vangstbm-153 has ommatidium phenotype, non-enhanceable by dlg1[+]/dlg118
Vangstbm-153 has ommatidium phenotype, non-enhanceable by dlg1[+]/dlg113
Vangstbm-153 has ommatidium phenotype, non-enhanceable by dlg1[+]/dlg1w55
Vangstbm-153 has ommatidium phenotype, non-enhanceable by l(2)gl4w3/l(2)gl[+]
Vangstbm-153 has ommatidium phenotype, non-enhanceable by par-6[+]/par-6Δ226
Vangstbm-153 has ommatidium phenotype, non-enhanceable by baz4/baz[+]
Vangstbm-153 has ommatidium phenotype, non-enhanceable by sdtXP/sdt[+]
Vangstbm-153 has ommatidium phenotype, suppressible by fred[+]/fredH24
Vangstbm-153 has ommatidium phenotype, non-suppressible by sdtXP/sdt[+]
Vangstbm-153 has ommatidium phenotype, non-suppressible by dlg1[+]/dlg114
Vangstbm-153 has ommatidium phenotype, non-suppressible by dlg1[+]/dlg118
Vangstbm-153 has ommatidium phenotype, non-suppressible by dlg1[+]/dlg113
Vangstbm-153 has ommatidium phenotype, non-suppressible by dlg1[+]/dlg1w55
Vangstbm-153 has ommatidium phenotype, non-suppressible by l(2)gl4w3/l(2)gl[+]
Vangstbm-153 has ommatidium phenotype, non-suppressible by par-6[+]/par-6Δ226
Vangstbm-153 has ommatidium phenotype, non-suppressible by baz4/baz[+]
Vangstbm-153 is an enhancer of ommatidium phenotype of stanfrz3
Vangstbm-153/Vang[+] is a non-enhancer of eye phenotype of Nab2EP3716, Scer\GAL4GMR.PU
Vangstbm-153/Vang[+] is a non-suppressor of eye phenotype of Nab2EP3716, Scer\GAL4GMR.PU
Vangstbm-153, stanfrz3 has photoreceptor neuron phenotype
Heterozygosity for scrib1 or scrib673 enhances the frequency of ommatidia that show planar cell polarity defects in Vangstbm-153 homozygotes.
Heterozygosity for dlg114, dlg118, dlg113, dlg1w55, l(2)gl4w3, par-6Δ226, baz4 or sdtXP has no effect on the frequency of ommatidia that show planar cell polarity defects in Vangstbm-153 homozygotes.
fredH24 dominantly suppresses the phenotype of mis-rotation of ommatidia that is seen in Vangstbm-153 animals.
Homozygosity for bdg164 enhances the ommatidial polarity defects caused by homozygosity for Vangstbm-153.
32.9% of ommatidia in stanfrz3/stanfrz3, Vangstbm-153/+ animals exhibit polarity defects in the eye. 63.7% of ommatidia in stanfrz3/stanfrz3, Vangstbm-153/Vangstbm-153 animals exhibit polarity defects in the eye. They also have missing photoreceptor cells. 49.7% of ommatidia in pk1/pk1, Vangstbm-153/Vangstbm-153 animals exhibit polarity defects in the eye.
Vangstbm-153 is partially rescued by VangΔPBM.cCa