Gene Information: egl-30

Nameegl-30 View on WormBase
Species C. elegans
SequenceM01D7.7
Genetic positionI:-12.56 +/- 0.028 cM
Genomic positionI: 1835661..1841965

Strains carrying this gene

Strain Genotype Description
CE1047 egl-30(ep271) I. Dominant, gain-of-function mutation in egl-30; missense M244I. This strain cannot be distributed to commercial organizations. This strain cannot be used for any commercial purpose or for work on human subjects.
CG21 egl-30(tg26) I; him-5(e1490) V. Hyperactive. Small. Spicule protruder. Coiler. Throws males.
DA1077 egl-30(ad810) dpy-5(e61)/szT1 [lon-2(e678)] I; +/szT1 X. ad810 is homozygous lethal. ad810/+ is Egl and it suppresses gpb-2 (a.k.a. eat-11). In DA1077, heterozygotes are Egl. Strain throws Lon Males.
DA1084 egl-30(ad806) I. Egl. Semi-dominant suppressor of eat-11.
DA1096 egl-30(ad810)/szT1 [lon-2(e678)] I; +/szT1 X. ad810 is homozygous lethal. ad810/+ is Egl and it suppresses gpb-2 (a.k.a. eat-11). In DA1096, heterozygotes are Egl. Throws Lon males.
DA810 egl-30(ad810) gpb-2(ad541)/gpb-2(ad541) I. ad810 is homozygous lethal. ad810/+ is Egl and it suppresses gpb-2. gpb-2 phenotype is rather subtle: they are slightly starved, slightly longer than normal, and tend to be loopy in their movements (they make abnormally deep bends). Hets should be Egl and non-Eat. On most E. coli strains gpb-2 grows rather poorly, especially if the plates are older so that there is a thick and tough lawn. On such plates there will be a lot of gpb-2 larval arrest, and those that don't arrest will grow slowly. The hets should easily outgrow the gpb-2 homozygotes. [gpb-2 is also hypersensitive to the drug arecoline: they won't grow on 5 mM. The hets will grow even better than WT on 5 mM arecoline.] gpb-2(ad541) previously called eat-11(ad541).
DA823 egl-30(ad805) I. Suppressor of gpb-2 (a.k.a. eat-11) arecoline hypersensitivity. Unc. Egl.
DG2913 egl-30(ad810) I/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP, arrested hT2 aneuploids, and non-GFP ad810 homozygotes. Homozygous hT2[bli-4 let-? qIs48] inviable. Pick WT GFP and check for correct segregation of progeny to maintain.
JJ478 mex-3(zu155) egl-30(n686)/hT1 I; +/hT1 V. Heterozygotes are WT and segregate WT, Egls which give only dead eggs, dead eggs, and mid-larval lethals (hT1 homozygotes)
MT1434 egl-30(n686) I. Egg-laying defective. Retains late stage eggs. Semi-dominant. Unc-slow moving.
MT1520 egl-30(n715) I. Egl-forms bags of worms. Semidominant. Paralysed. Grows best at 15C.
MT2609 egl-30(n715n1190) I. Non-Egl.
NM1380 egl-30(js126) I. Suppresses unc-64(e246).
PS4263 egl-30(md186) I; dpy-20(e1282) IV; syIs105. syIs105 [egl-30::GFP + dpy-20(+)]. Translational fusion contains all of the presumptive 5'-transcriptional regulatory sequences, introns, and presumptive 3 regulatory sequences for egl-30, in addition to the coding sequences for GFP just 5' of the egl-30 initiating methionine. syIs105 was found to partially rescue egl-30(md186) with respect to egg laying, movement, pharyngeal pumping, and response to neurotransmitters in egg-laying assays.
PS4264 egl-30(sy676md186) I; him-5(e1490) V. Males mate better as heterozygotes. This strain cannot be distributed to commercial organizations. This strain cannot be used for any commercial purpose or for work on human subjects.
VC1160 egl-30&emr-1(ok252) I/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). M01D7.7, M01D7.6. Homozygous viable deletion chromosome balanced by bli-4- and GFP-marked translocation. Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP, arrested hT2 aneuploids, and non-GFP ok252 homozygotes (phenotype uncharacterized). Homozygous hT2[bli-4 let-? qIs48] inviable. Pick WT GFP and check for correct segregation of progeny to maintain. Attribution: This strain was provided by the C. elegans Reverse Genetics Core Facility at the University of British Columbia, which is part of the international C. elegans Gene Knockout Consortium, which should be acknowledged in any publications resulting from its use. Paper_evidence WBPaper00041807