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Strain Species Genotype
MQ29 C. elegans mau-3(qm10) IV. Show Description
Maternal effect uncoordinated. Progressive paralysis. Abnorml muscle anatomy. Some embryonic and larval lethality.
MQ475 C. elegans mau-5(qm17) III. Show Description
Maternal effect uncoordinated. Progressively worsening sluggishness and saccidic forward movement. Egg laying defective. Abnormal muscle anatomy. Some embryonic and larval lethality.
MQ770 C. elegans tpk-1(qm162) III. Show Description
Maternal effect slow growing.
MQ809 C. elegans dpy-17(e164) dec-7(qm166) III. Show Description
Dpy. Fast defecation.
MQ853 C. elegans mau-2(qm160) I. Show Description
100% Unc. 100% Egl. 15% Lid.
MQ876 C. elegans daf-2(e1370) III; isp-1(qm150) IV. Show Description
Slow development rate. Dauer constitutive at 25C. Grow at 15C.
MQ887 C. elegans isp-1(qm150) IV. Show Description
Slow development and behavior. Grows better at 15C.
MQ920 C. elegans dsc-4(qm182) IV. Show Description
Defecation suppressor of clk-1(qm30).
MQ989 C. elegans isp-1(qm150) IV; ctb-1(qm189). Show Description
Slow post-embryonic development and behavior.
MQ992 C. elegans coq-3(qm188)/dpy-4(e1166) IV. Show Description
Heterozygotes are WT and segregate WT, Dpys, and Steriles.
MS662 C. elegans tbx-35(tm1789) II; irEx274. Show Description
irEx274 [ZK177 + unc-119::CFP + rol-6(su1006)]. Maintain by picking Rollers. Strain throws Rollers (expressing unc-119::CFP), dead eggs, and developmentally-arrrested L1s. Roller is often weak or not apparent. A greater proportion of tbx-35(tm1789) embryos will hatch as inviable L1s at 15C as compared with 20C or 25C.
MT15062 C. elegans hpl-2(tm1489) III; hpl-1(n4317) X. Show Description
MT15606 C. elegans met-2(n4256) hpl-2(tm1489) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). Show Description
Heterozygotes are WT and GFP+. qIs48 [myo-2::GFP + pes-10::GFP + ges-1::GFP]. Homozygous hT2 animals are inviable. May have lin-15A(n767) in background.
MT16429 C. elegans set-6(tm1611) lin-15A(n767) X. Show Description
Reference: Andersen EC & Horvitz HR., Development. 2007 Aug;134(16):2991-9.
MT16430 C. elegans set-6(tm1611) lin-15B(n744) X. Show Description
Reference: Andersen EC & Horvitz HR., Development. 2007 Aug;134(16):2991-9.
NB105 C. elegans fcd-2(tm1298) IV. Show Description
Homozygotes are viable, but are hypersensitive to DNA crosslinks.
NB131 C. elegans wrn-1(gk99)/mIn1[dpy-10(e128) mIs14(GFP)] II; exo-1(tm1842) III. Show Description
Heterozygotes (wrn-1/mIn1;exo-1) are WT and GFP+. mIn1 homozygotes (mIn1;exo-1) are Dpy and GFP+. wrn-1;exo-1 homozygotes are non-GFP.  Reference: Ryu, J.S. and Koo, H.S. (2017). FEBS Lett.
NB245 C. elegans aak-1(tm1944) III; aak-2(gt33) X. Show Description
Hypersensitive to oxidative stress; more sensitive to the stress than either of the cognate single mutants. Parental aak-1(tm1944) strain outcrossed 8 times; parental aak-2(gt33) strain outcrossed 3 times. Reference: Lee H, et al. J Biol Chem. 2008 May 30;283(22):14988-93.
NB327 C. elegans ints-6(tm1615) IV/nT1 [qIs51] (IV;V). Show Description
Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP+, arrested nT1 aneuploids, and non-GFP dic-1 homozygotes. dic-1(tm1615) homozygotes arrest at the L3 larval stage. ints-6 previously known as dic-1.
NB390 C. elegans hsr-9(ok759) I; brc-1(tm1145) III. Show Description
Reduced apoptosis after gamma-ray treatment compared to N2. Double mutant exhibits hypersensitivity to gamma rays similar to brc-1(tm1145) alone. Reference: Ryu JS, et al; PLoS One. (In Press).
NB514 C. elegans exo-1(tm1842) III; parg-2(ok980) IV. Show Description
Double mutant is less sensitive to ionizing radiation than the parg-2(ok980) single mutant, but as sensitive as the exo-1(tm1842) single mutant. Parental parg-2(ok980) strain outcrossed 6 times; parental exo-1(tm1842) strain outcrossed 4 times. Reference: Bae W, et al. Hypersensitivity to DNA double-strand breaks associated with PARG deficiency is suppressed by exo-1 and polq-1 mutations in Caenorhabditis elegans. The FEBS Journal, In press.
NG103 C. elegans mig-2(gm103) X. Show Description
Severe Unc. Some withered tails. Occasional lateral vulvae. Semi-dominant allele.
NG126 C. elegans syc-1(gm126) III. Show Description
Recessive. Maternal rescue Dpy. Slightly Unc. Small broods. CAN migration nearly normal in absence of kyIs5.
NG132 C. elegans syc-2(gm132) X. Show Description
Unc. Recessive. CAN migration nearly normal in absence of kyIs5.
NG135 C. elegans syc-3(gm135) I. Show Description
Weak loopy Unc. CAN migration mostly normal in absence of kyIs5 reporter.
NG144 C. elegans ina-1(gm144) III. Show Description
Pvul, occasional lateral vulvae. CAN migration defective.
NG2473 C. elegans unc-73(gm123) I; sDp2 (I;f). Show Description
Animals with sDp2 are WT. Animals without the duplication are severe Uncs with withered tails, are small and often have lateral ectopic vulvae. gm123 does not survive through more than 1-2 generations. Many cell migrations defects in gm123 animals.
NG2501 C. elegans epi-1(gm121) kyIs5 IV. Show Description
kyIs5 [ceh-23p::unc-76::GFP + lin-15(+)] IV. kyIs5 contains a fragment of unc-76 protein that drives enrichment of GFP in the axons.
NG2535 C. elegans cam-2(gm124) I. Show Description
Recessive. Small, moderate Unc. 10% Muv. CAN cell migration defects. Clr.
NG2615 C. elegans cam-1(gm122) II. Show Description
NM1081 C. elegans snb-1(js124)/dpy-11(e224) unc-68(r1158) V. Show Description
Heterozygotes are WT and segregate WT, DpyUncs and L1 lethals. js124 homozygotes arrest as L1 larvae that are very uncoordinated and tend to adopt a coiled position. js124 molecular lesion is an amber mutation at codon 50.
NM1233 C. elegans jsIs219 II. Show Description
jsIs219 [(pSY3) sng-1::GFP + rol-6(su1006)]. Rollers.
NM1278 C. elegans rbf-1(js232) III. Show Description
Lethargic in the absence of stimulation. 1500 bp deletion including the promoter and first three exons of C. elegans rabphilin homolog.
NM1378 C. elegans unc-43(js125) V. Show Description
Unc. Maintain under normal conditions. Reference: Hawasli A, et al. Genetics. 2004 Oct;168(2):831-43.
NM1380 C. elegans egl-30(js126) I. Show Description
Suppresses unc-64(e246).
NM1448 C. elegans jsIs37 rpm-1(js410) V. Show Description
jsIs37 [mec-7p::snb-1::GFP) + lin-15(+)]. Superficially wild-type. snb-1::GFP expression in a subset of mechanosensory neurons; GFP is faint and can only be seen on a compound microscope. Reduced SNB-1::GFP localization to synaptic regions; slighty Dpy. js410 has linked phenotype of reduced brood size. js410 is an R->Stop at aa 235. snb-1::GFP is expressed in mechanosensory neurons visible in the cell body and in the axon (very low levels). GFP puncta absent from the ventral nerve cord due to rpm-1 lesion.
NM1455 C. elegans jsIs37 rpm-1(js317) V. Show Description
jsIs37 [mec-7p::snb-1::GFP) + lin-15(+)]. Superficially wild-type. snb-1::GFP expression in a subset of mechanosensory neurons; GFP is faint and can only be seen on a compound microscope. Reduced SNB-1::GFP localization to synaptic regions; slighty Dpy. js317 is a W->Stop at aa 861. snb-1::GFP is expressed in mechanosensory neurons visible in the cell body and in the axon (very low levels). GFP puncta absent from the ventral nerve cord due to rpm-1 lesion.
NM1489 C. elegans dhc-1(js319) I; jsIs37 V. Show Description
jsIs37 [mec-7p::snb-1::GFP) + lin-15(+)]. Superficially wild-type. snb-1::GFP expression in a subset of mechanosensory neurons; GFP is faint and can only be seen on a compound microscope.May be slightly Unc. dch-1 alias sam-11.
NM1568 C. elegans ehs-1(ok146) II. Show Description
An approx. 1-8 kb deletion in the ZK1248.3 gene which encodes a C. elegans homolog of the Eps15 (vertebrate) and pan1 (S. cervesisiae) gene. No obvious behavioral or morphological phenotypes.
NM1581 C. elegans rpy-1(ok145) II. Show Description
Viable, fertile, with no obvious behavioral or morphological phenotypes. A 1677 bp deletion in the C18H9.7 gene which encodes a C. elegans homolog of the rapysn (vertebrate) gene. The lesion deletes exons 4 through 10, leaving exons 3 and 11 in frame. The deletion junction is cagaagaaaaagttcgctttgaactaaAGAACCTATTGAAAATTCTTACTT. Previously called rap-1.
NM1630 C. elegans slo-1(js118) III. Show Description
Mutants are hyperactive and hypersensitive to aldicarb.
NM1657 C. elegans unc-10(md1117) X. Show Description
Uncoordinated and aldicarb resistant. Molecular lesion: deletion of entire unc-10 coding region. Gene encodes C. elegans homolog of Rab3 interacting molecule. Will mate, but poorly.
NM1815 C. elegans tom-1(ok188) I. Show Description
NM1968 C. elegans slo-1(js379) V. Show Description
Jerky locomotion. Sensitive to aldicarb.
OC271 C. elegans pph-4.1(tm1598) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). Show Description
Homozygous sterile mutation 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 tm1598 homozygotes (produce ~100% dead eggs, slightly higher penetrance at 25C). Homozygous hT2[bli-4 let-? qIs48] inviable. Pick WT GFP and check for correct segregation of progeny to maintain. Reference: Peters N, et al., J Cell Sci. 2010 Mar 1;123(Pt 5):795-805.
OE3001 C. elegans him-8(e1489) IV; dyf-4(m158) V. Show Description
Defective in dye filling (FITC or DiO) of amphid and phasmid neurons. Chemotaxis defective. Throws males.
OE3002 C. elegans him-8(e1489) IV; xbx-1(ok279) V. Show Description
Dyf. Osm. Throws males. Reduced mating efficiency (ME 2-3). Deletion extends over 1610 bp in the intron between exons 3 and 4 and ending 30 bp after the STOP codon (cosmid F02D8 pb 25954-27563 are deleted). Complements dyf-4(m158).
OH11416 C. elegans otIs419. Show Description
otIs419 [snb-1p(prom17)::2xNLS::GFP + elt-2::DsRed2]. Ubiquitous GFP expression. Reference: Stefanakis N., Carrera I., Hobert O. Neuron. 2015 Aug 19;87(4):733-50.
OH12503 C. elegans otIs520 X. Show Description
otIs520 [eat-4(prom11)::GFP + ttx-3::mCherry] X. AIM is marked only with GFP, not mCherry. Can be used to isolate AIM by FACS. Used by CeNGEN project for RNA-Seq (https://www.cengen.org/).
OH14018 C. elegans him-5(e1490) V; otIs520. Show Description
otIs520 [eat-4(prom11)::GFP + ttx-3::mCherry]. Reference: Serrano-Saiz E, et al. Curr Biol. 2017 Jan 23;27(2):199-209.