| CF162 |
C. elegans |
mig-2(mu28) X. Show Description
mig-2 null mutation. Animals look grossly WT but Q descendants and other migratory neurons misplaced.
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| LE815 |
C. elegans |
mig-2(lq13) X. Show Description
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| NG103 |
C. elegans |
mig-2(gm103) X. Show Description
Severe Unc. Some withered tails. Occasional lateral vulvae. Semi-dominant allele.
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| NG2475 |
C. elegans |
mig-2(gm38) X. Show Description
Unc. Recessive allele for most phenotypes. Appears to be a gain of function mutation (see Zipkin et al. 1997).
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| RB1769 |
C. elegans |
mig-2(ok2273) X. Show Description
C35C5.4. Homozygous. Outer Left Sequence: CCGAGGTTTTCGTTTTTCAA. Outer Right Sequence: AATGACTGGGAAACGTCCAA. Inner Left Sequence: TTTTGTTCCACGCTTTGTCA. Inner Right Sequence: ATGATCGGGAAGAAGAGCCT. Inner Primer PCR Length: 2116 bp. Deletion Size: 1192 bp. Deletion left flank: ATTTTCGCCAACTTTTCATTCCCTAACTTT. Deletion right flank: TTTTGTTGAAACTCATAAAACTATATCTTG. Attribution: This strain was provided by the C. elegans Gene Knockout Project at the Oklahoma Medical Research Foundation, which was part of the International C. elegans Gene Knockout Consortium, which should be acknowledged in any publications resulting from its use. Paper_evidence WBPaper00041807
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| LE554 |
C. elegans |
mig-2(mu28) lqIs2 X. Show Description
lqIs2 [osm-6::GFP] X. lqIs2 carries a PDE/amphid/phasmid marker linked to mig-2. Reference: Struckhoff EC, Lundquist EA. Development 2003, 130:693-704.
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| LE1112 |
C. elegans |
tiam-1(ok772) I; mig-2(mu28) lqIs2 X. Show Description
lqIs2 [osm-6::GFP + lin-15(+)]. Maintain under normal conditions. Reference: Demarco RS, Struckhoff EC, Lundquist EA. PLoS Genetics 2011.
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| LE2514 |
C. elegans |
tiam-1(tm1556) I; mig-2(mu28) lqIs2 X. Show Description
lqIs2 [osm-6::GFP + lin-15(+)]. Maintain under normal conditions. Reference: Demarco RS, Struckhoff EC, Lundquist EA. PLoS Genetics 2011.
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| LE3190 |
C. elegans |
tiam-1(tm1556) I; juIs76 II; mig-2(mu28) lqIs2 X. Show Description
juIs76 [unc-25p::GFP + lin-15(+)] II. lqIs2 [osm-6::GFP] X. lqIs2 carries a PDE/amphid/phasmid marker linked to mig-2. Reference: Demarco RS, et al. PLoS Genet. 2012;8(4):e1002665.
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| LE3192 |
C. elegans |
tiam-1(ok772) I; juIs76 II; mig-2(mu28) lqIs2 X. Show Description
juIs76 [unc-25p::GFP + lin-15(+)] II. lqIs2 [osm-6::GFP] X. lqIs2 carries a PDE/amphid/phasmid marker linked to mig-2. Reference: Demarco RS, et al. PLoS Genet. 2012;8(4):e1002665.
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| CF579 |
C. elegans |
dpy-20(e1282) IV; him-5(e1490) V; muIs27. Show Description
muIs27 [mig-2::GFP + dpy-20(+)]. Him. non-Dpy. GFP is membrane enriched and expressed in many cells throughout development (see reference for details). Not known in which LG muIs27 is integrated.
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| CF693 |
C. elegans |
unc-31(e169) IV; him-5(e1490) V; muIs28. Show Description
muIs28 [mig-2::GFP + unc-31(+)]. muIs28 is not mapped, but probably on LG II by process of elimination.
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| NF1226 |
C. elegans |
mig-22(tk69) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). Show Description
mig-22(tk69): DTC migration defect and maternal effect embryonic lethal. Heterozygotes are WT with pharyngeal GFP signal. Homozygous hT2[bli-4 let-? qIs48] are inviable.
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| NF317 |
C. elegans |
mig-23(k180) X. Show Description
Distal tip cell migration defective. Tc1 insertion mutant. Spontaneous mutant with ventral white patch phenotype.
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| NF591 |
C. elegans |
mig-22(tk24) III. Show Description
DTC migration defect.
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| NF68 |
C. elegans |
mig-22(k141) III. Show Description
DTC migration defect.
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| NF78 |
C. elegans |
mig-20(k148) X. Show Description
Distal tip cell, HSN, left cc mother cell, QR(d) migration defective.
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| TU2461 |
C. elegans |
mig-21(u787) III. Show Description
Abnormal migration of AVM and PVM cells.
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