Laboratory Information

NameFX View on WormBase
Allele designationtm
HeadShohei Mitani
InstitutionTokyo Women's Medical University School of Medicine, Tokyo, Japan
Address Department of Physiology
Tokyo Women's Medical University
8-1, Kawada-cho
Shinjuku-ku 162-8666
Japan
Gene classes ift  inos  rabs  bcl  tlg 

Strains contributed by this laboratory

Strain Genotype Species Description
FX1053 ins-11(tm1053) II. C. elegans Superficially wild type. Attribution: This strain was generated by the National Bioresource Project at the Tokyo Women's Medical University School of Medicine, 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
FX11364 pps-1(tm1109)/mec-3(u297) IV. C. elegans Heterozygotes are WT and segregate WT, Mec and larval lethals. Attribution: This strain was generated by the National Bioresource Project at the Tokyo Women's Medical University School of Medicine, 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
FX11501 dpy-5(e61) uri-1(tm939)/dpy-5(e61) unc-14(e57) I. C. elegans Heterozygotes are Dpy. Segregate Dpy Unc. tm939 homozygotes are emb, leth, pvl, rup, larval arrested or sterile. Attribution: This strain was generated by the National Bioresource Project at the Tokyo Women's Medical University School of Medicine, 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
FX11507 rabs-5(tm2036) IV/nT1 [qIs51] (IV;V). C. elegans Heterozygotes are WT with pharyngeal GFP signal, and segregate arrested nT1 aneuploids, and non-GFP tm2036 homozygotes. tm2036 homozygotes are temperature sensitive lethal, and can be maintained as homozygotes at 15C. tm2036 homozygotes have endocytosis defects in oocytes and coelomocytes at 25C. Attribution: This strain was generated by the National Bioresource Project at the Tokyo Women's Medical University School of Medicine, 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
FX11552 vps-45(tm246)/egl-17(e1313) lon-2(e678) X. C. elegans Heterozygotes are WTand segregate WT, Egl Lon, and tm246 homozygotes (temperature sensitive lethal which can be maintained as homozygotes at 15C). tm246 homozygotes have endocytosis defects in oocytes and coelomocytes at 25C. Attribution: This strain was generated by the National Bioresource Project at the Tokyo Women's Medical University School of Medicine, 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
FX1524 cku-70(tm1524) III. C. elegans Attribution: This strain was generated by the National Bioresource Project at the Tokyo Women's Medical University School of Medicine, 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
FX17650 lin-1(tm5929)/tmIn1 IV. C. elegans Homozygous lethal or sterile deletion allele balanced by Unc-marked translocation. Break points: In(egl-4 unc-17) IV. Covered region (Mb) 1.8 (1.8..3.6) Unc. Reference: Iwata S, et al. Sci Rep. 2016 Sep 21;6:33840.
FX17788 mlt-7(tm1794)/tmIn4 II. C. elegans Heterozygotes are slightly Dpy, and segregate slightly Dpy mlt-7/tmIn4 heterozygotes, Dpy tmIn4 homozygotes, and mlt-7(tm1794) homozygotes (Let). Break points: In(lin-8 dpy-2) II. Covered region (Mb) 3.7 (3.1..6.7) Dpy. Reference: Iwata S, et al. Sci Rep. 2016 Sep 21;6:33840.
FX19059 Y38F2AR.9(tm1986)/tmIn3 IV. C. elegans Homozygous lethal deletion allele balanced by Unc-marked translocation. Break points: In(jtr-1 unc-17) IV. Covered region (Mb) 2.2 (1.4..3.6) Unc. Reference: Iwata S, et al. Sci Rep. 2016 Sep 21;6:33840.
FX19119 atm-1(tm5027) C46H11.6(tm7811) I; tmIn20 II; xpc-1(tm3886) F01D4.9(tm7812) IV; aqp-4(tm7813) V. C. elegans tmIn20 is an inversion between F46C5.9 and C08H9.13 in LG II.  Inversion strain obtained by Next-generation sequencing.
FX19120 atm-1(tm5027) Y47G6A.28(tm7889) nepr-1(tm7890) I; C18H9.6(tm7891) II; xpc-1(tm3886) tmIn21 IV; srh-54(tm7892) V. C. elegans tmIn21 is an inversion between pck-3 and R09H10.5 in LG IV.  Inversion strain obtained by Next-generation sequencing.
FX19134 tmIn8 II. C. elegans Break points: In(F13D12.6 Y51H1A.2) II. Covered region (Mb) 2.1 (11.7..13.9) Obtained by TMP/UV. (Note: Y51H1A.2 has been renamed cup-14.) [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX19141 atm-1(tm5027) C37A2.6(tm8115) I; Y48A6B.8(tm8116) III; xpc-1(tm3886) IV; tmIn22 V. C. elegans tmIn22 is an inversion between W02G9.9 and 21ur-15544 in LG V.  Inversion strain obtained by Next-generation sequencing.
FX19161 dpy-20(tm5940)/tmIn5 IV. C. elegans Homozygous lethal or sterile deletion allele balanced by Unc-marked translocation. Break points: In(mec-3 unc-31) IV. Covered region (Mb) 2.3 (10.5..12.8) Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX19163 mca-3(tm6395)/tmIn11 IV. C. elegans Homozygous lethal deletion allele balanced by Unc-marked translocation. Heterozygotes are wild-type and segregate wild-type heterozygotes, lethal tm6395 homozygotes, and Unc tmIn11 homozygotes. Break points: In(kvs-5 unc-17) IV. Covered region (Mb) 2.9 (0.7..3.6) [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX19170 lin-1(tm5929)/tmIn2 IV. C. elegans Homozygous lethal or sterile deletion allele balanced by Unc-marked translocation. Break points: In(ced-2 unc-17) IV. Covered region (Mb) 2 (1.6..3.6) Unc. Reference: Iwata S, et al. Sci Rep. 2016 Sep 21;6:33840.
FX19171 lig-4(tm750) III; tmIn26 X. C. elegans tmIn26 homozygotes are Lon and Mec. Break points: In(lon-2 mec-10) X. Covered region (Mb) 3.7 (4.7..8.5) Lon Mec. [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Iwata S, et al. Sci Rep. 2016 Sep 21;6:33840.
FX19173 lig-4(tm750); tmIn19 V. C. elegans Break points: In(unc-23 lon-3) V. Covered region (Mb) 3.3 (8.9..12.2) Lon Unc. [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX19181 unc-15(tm6329)/tmIn14 I. C. elegans Homozygous lethal deletion allele balanced by Dpy-marked translocation. Break points: In(dpy-5 lin-10) I. Covered region (Mb) 2.7 (5.4..8.1) Dpy. [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX19397 tmC1 X; tmEx4487. C. elegans tmEx4487 [unc-18(+) + myo-2p::Venus]. Break points: In(F53B1.2 unc-18 In(lon-2 mec-10)) X. Covered region (Mb) 6.4 (2.1..8.5) Lon Mec (Unc). Pick fluorescent non-Unc to maintain array. Males carrying the array (Venus in pharynx) can mate. Reference: Iwata S, et al. Sci Rep. 2016 Sep 21;6:33840.
FX19472 tmIn10 II. C. elegans Break points: In(ZK1240.1 F29A7.8) II. Covered region (Mb) 0.4 (2.3..2.8) Obtained by TMP/UV. [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX19584 lig-4(tm750) III; tmIn51 IV. C. elegans tmIn51 is a CRISPR/Cas9-induced inversion between C09G12.5 and C01B10.3 in LG IV.
FX19585 lig-4(tm750) tmIn52 III. C. elegans Break points: In(hpr-9 ttr-52) III. Covered region (Mb) 2.8 (10.6..13.4) [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX19666 tmC5 IV. C. elegans Break points: In(C01B10.3 eak-7 In(mec-3 unc-31)) IV. Covered region (Mb) 6.2 (6.6..12.8) Mec Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX19668 tmC6 [dpy-2(tmIs1189)] II. C. elegans Break points: In(sri-57 asm-1 In(ZK1240.1 F29A7.8)) II. Covered region (Mb) 4.6 (2.3..6.9) Balancer marked with myo-2p::Venus. Dpy. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX19702 lig-4(tm750) III; tmIn54 V. C. elegans Break points: In(srbc-66 T10H9.8) V. Covered region (Mb) 3.1 (3.5..6.7) [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX19704 tmIn58 I; lig-4(tm750) III. C. elegans Break points: In(gsp-3 sre-23) I. Covered region (Mb) 3.5 (4.7..8.3) [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX19706 lig-4(tm750) III; tmIn60 X. C. elegans Break points: In(odr-7 F59F4.2) X. Covered region (Mb) 3.4 (12.5..15.8) Unknown if tmIn60 homozygotes are Odr. [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX19992 lig-4(tm750); tmIn62 IV. C. elegans Break points: In(kvs-5 dmd-9) IV. Covered region (Mb) 2.5 (0.7..3.3) [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX2355 ift-81(tm2355) X. C. elegans Superficially WT. Attribution: This strain was generated by the National Bioresource Project at the Tokyo Women's Medical University School of Medicine, 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
FX2394 ift-74(tm2394) II. C. elegans Superficially WT. Attribution: This strain was generated by the National Bioresource Project at the Tokyo Women's Medical University School of Medicine, 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
FX291 +/eT1 III; spn-4(tm291)/eT1 V. C. elegans Heterozygotes are WT and segregate WT, Unc-36 and dead eggs. 1/3 of WT animals (spn-4 homozygotes) are Mels: segregate only dead embryos with have no morphogenesis. Attribution: This strain was generated by the National Bioresource Project at the Tokyo Women's Medical University School of Medicine, 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
FX30123 tmC24 [F23D12.4(tmIs1233)] X. C. elegans Break points: In(mec-10 Y7A5A.20 In(odr-7 F59F4.2)) X. Covered region (Mb) 7.4 (8.5..15.8) Balancer marked with myo-2p::mCherry. Mec. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30126 tmC1 X. C. elegans Break points: In(F53B1.2 unc-18 In(lon-2 mec-10)) X. Covered region (Mb) 6.4 (2.1..8.5) Lon Unc Mec. Reference: Iwata S, et al. Sci Rep. 2016 Sep 21;6:33840.
FX30133 tmC3 V. C. elegans Break points: In(unc-83 C27A7.1 In(unc-23 lon-3)) V. Covered region (Mb) 5.7 (6.5..12.2) Lon Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30134 tmC3 [egl-9(tmIs1228)] V. C. elegans Break points: In(unc-83 C27A7.1 In(unc-23 lon-3)) V. Covered region (Mb) 5.7 (6.5..12.2) Balancer marked with myo-2p::Venus. Lon Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30135 tmC3 [egl-9(tmIs1230)] V. C. elegans Break points: In(unc-83 C27A7.1 In(unc-23 lon-3)) V. Covered region (Mb) 5.7 (6.5..12.2) Balancer marked with myo-2p::mCherry. Lon Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30138 tmC6 [dpy-2(tmIs1208)] II. C. elegans Break points: In(sri-57 asm-1 In(ZK1240.1 F29A7.8)) II. Covered region (Mb) 4.6 (2.3..6.9) Balancer marked with myo-2p::mCherry. Dpy. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30140 tmC5 [F36H1.3(tmIs1220)] IV. C. elegans Break points: In(C01B10.3 eak-7 In(mec-3 unc-31)) IV. Covered region (Mb) 6.2 (6.6..12.8) Balancer marked with myo-2p::Venus. Mec Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30143 tmC6 II. C. elegans Break points: In(sri-57 asm-1 In(ZK1240.1 F29A7.8)) II. Covered region (Mb) 4.6 (2.3..6.9) Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30144 tmC6 [dpy-2(tm9710)] II. C. elegans Break points: In(sri-57 asm-1 In(ZK1240.1 F29A7.8)) II. Covered region (Mb) 4.6 (2.3..6.9) Dpy. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30151 tmC9 IV. C. elegans Break points: In(glb-19 lgc-52 In(mec-3 unc-31)) IV. Covered region (Mb) 4.8 (10.5..15.2) Unc Mec. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30152 tmC12 [egl-9(tmIs1194)] V. C. elegans Break points: In(hlh-10 C01G10.10 In(unc-23 lon-3)) V. Covered region (Mb) 6.1 (8.9..15.1) Balancer marked with myo-2p::Venus. Lon Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30153 tmC12 [egl-9(tmIs1197)] V. C. elegans Break points: In(hlh-10 C01G10.10 In(unc-23 lon-3)) V. Covered region (Mb) 6.1 (8.9..15.1) Balancer marked with myo-2p::mCherry. Lon Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30154 tmC12 V. C. elegans Break points: In(hlh-10 C01G10.10 In(unc-23 lon-3)) V. Covered region (Mb) 6.1 (8.9..15.1) Lon Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30161 tmC16 [unc-60(tmIs1237)] V. C. elegans Break points: In(flp-34 C04E6.7 In(srbc-66 T10H9.8)) V. Covered region (Mb) 5.6 (1..6.7) Balancer marked with myo-2p::mCherry. Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30162 tmC16 V. C. elegans Break points: In(flp-34 C04E6.7 In(srbc-66 T10H9.8)) V. Covered region (Mb) 5.6 (1..6.7) Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30164 tmC16 [unc-60(tm9712)] V. C. elegans Break points: In(flp-34 C04E6.7 In(srbc-66 T10H9.8)) V. Covered region (Mb) 5.6 (1..6.7) Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30166 tmC18 I. C. elegans Break points: In(B0207.10 dnj-27 In(gsp-3 sre-23)) I. Covered region (Mb) 7.2 (4.7..11.9) Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30167 tmC18 [dpy-5(tmIs1200)] I. C. elegans Break points: In(B0207.10 dnj-27 In(gsp-3 sre-23)) I. Covered region (Mb) 7.2 (4.7..11.9) Balancer marked with myo-2p::Venus. Dpy. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30168 tmC18 [dpy-5(tmIs1236)] I. C. elegans Break points: In(B0207.10 dnj-27 In(gsp-3 sre-23)) I. Covered region (Mb) 7.2 (4.7..11.9) Balancer marked with myo-2p::mCherry. Dpy. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30176 tmC20 I. C. elegans Break points: In(F53G12.8 T02E1.7 In(gsp-3 sre-23)) I. Covered region (Mb) 8.1 (0.1..8.3) Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30177 tmC20 [unc-14(tmIs1219)] I. C. elegans Break points: In(F53G12.8 T02E1.7 In(gsp-3 sre-23)) I. Covered region (Mb) 8.1 (0.1..8.3) Balancer marked with myo-2p::Venus. tmIs1219 is inserted in unc-14, but Unc phenotype is not detectable. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30179 tmC20 [unc-14(tmIs1219) dpy-5(tm9715)] I. C. elegans Break points: In(F53G12.8 T02E1.7 In(gsp-3 sre-23)) I. Covered region (Mb) 8.1 (0.1..8.3) Balancer marked with myo-2p::Venus. Dpy. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30185 tmC24 X. C. elegans Break points: In(mec-10 Y7A5A.20 In(odr-7 F59F4.2)) X. Covered region (Mb) 7.4 (8.5..15.8) Mec. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30186 tmC24 [F23D12.4(tmIs1233) unc-9(tm9718)] X. C. elegans Break points: In(mec-10 Y7A5A.20 In(odr-7 F59F4.2)) X. Covered region (Mb) 7.4 (8.5..15.8) Balancer marked with myo-2p::mCherry. Unc Mec. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30194 tmC24 [F23D12.4(tmIs1240) unc-9(tm9719)] X. C. elegans Break points: In(mec-10 Y7A5A.20 In(odr-7 F59F4.2)) X. Covered region (Mb) 7.4 (8.5..15.8) Balancer marked with myo-2p::Venus. Unc Mec. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30197 tmC25 IV. C. elegans Break points: In(mak-2 unc-8 In(kvs-5 dmd-9)) IV. Covered region (Mb) 6.5 (0.7..7.2) One breakpoint is in unc-8, but Unc phenotype is not detectable. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30203 tmC25 [unc-5(tmIs1241)] IV. C. elegans Break points: In(mak-2 unc-8 In(kvs-5 dmd-9)) IV. Covered region (Mb) 6.5 (0.7..7.2) Balancer marked with myo-2p::Venus. Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30205 tmC27 I. C. elegans Break points: In(ile-1 Y18D10A.2 In(dnj-27 dkf-1)) I. Covered region (Mb) 4 (9.6..13.6) Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30208 tmC27 [unc-75(tmIs1239)] I. C. elegans Break points: In(ile-1 Y18D10A.2 In(dnj-27 dkf-1)) I. Covered region (Mb) 4 (9.6..13.6) Balancer marked with myo-2p::Venus. Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30218 tmC30 [ubc-17(tmIs1247)] X. C. elegans Break points: In(Y102A11A.6 R09F10.1 In(lon-2 mec-10)) X. Covered region (Mb) 6.4 (2..8.5) Balancer marked with myo-2p::Venus. Lon Mec. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30225 tmIn65; lig-4(tm750) I. C. elegans Break points: In(dnj-27 dkf-1) I. Covered region (Mb) 1.8 (11.9..13.6) [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30227 tmC29 III. C. elegans Break points: In(hlh-4 Y39E4A.1 In(hpr-9 ttr-52)) III. Covered region (Mb) 3.7 (9.7..13.4) semi-Emb. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30229 tmC30 X. C. elegans Break points: In(Y102A11A.6 R09F10.1 In(lon-2 mec-10)) X. Covered region (Mb) 6.4 (2..8.5) Lon Mec. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30233 tmC16 [unc-60(tmIs1210)] V. C. elegans Break points: In(flp-34 C04E6.7 In(srbc-66 T10H9.8)) V. Covered region (Mb) 5.6 (1..6.7) Balancer marked with myo-2p::Venus. Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30234 tmC9 [F36H1.2 (tmIs1221)] IV. C. elegans Break points: In(glb-19 lgc-52 In(mec-3 unc-31)) IV. Covered region (Mb) 4.8 (10.5..15.2) Balancer marked with myo-2p::Venus. Unc Mec. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30235 tmC20 [dpy-5(tm9709)] I. C. elegans Break points: In(F53G12.8 T02E1.7 In(gsp-3 sre-23)) I. Covered region (Mb) 8.1 (0.1..8.3) Dpy. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30236 tmC30 [ubc-17(tmIs1243)] X. C. elegans Break points: In(Y102A11A.6 R09F10.1 In(lon-2 mec-10)) X. Covered region (Mb) 6.4 (2..8.5) Balancer marked with myo-2p::mCherry. Lon Mec. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30237 tmC24 [unc-9(tm9723)] X. C. elegans Break points: In(mec-10 Y7A5A.20 In(odr-7 F59F4.2)) X. Covered region (Mb) 7.4 (8.5..15.8) Unc Mec. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30238 tmC18 [dpy-5(tm9705)] I. C. elegans Break points: In(B0207.10 dnj-27 In(gsp-3 sre-23)) I. Covered region (Mb) 7.2 (4.7..11.9) Dpy. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30240 tmC24 [F23D12.4(tmIs1240)] X. C. elegans Break points: In(mec-10 Y7A5A.20 In(odr-7 F59F4.2)) X. Covered region (Mb) 7.4 (8.5..15.8) Balancer marked with myo-2p::Venus. Mec. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30252 tmC24 [F23D12.4(tmIs1240) unc-9(tm9719)] X; tmEx4950. C. elegans tmEx4950 [unc-9(+) + vha-6p::GFP]. Break points: In(mec-10 Y7A5A.20 In(odr-7 F59F4.2)) X. Covered region (Mb) 7.4 (8.5..15.8) Balancer marked with myo-2p::Venus. Mec (Unc). Pick non-Unc GFP+ to maintain array. Males carrying the array (intestinal GFP) can mate. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30253 tmC24 [F23D12.4(tmIs1233) unc-9(tm9718)] X; tmEx4950. C. elegans tmEx4950 [unc-9(+) + vha-6p::GFP]. Break points: In(mec-10 Y7A5A.20 In(odr-7 F59F4.2)) X. Covered region (Mb) 7.4 (8.5..15.8) Balancer marked with myo-2p::mCherry. Mec (Unc). Pick non-Unc GFP+ to maintain array. Males carrying the array (intestinal GFP) can mate. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30257 tmC25 [unc-5(tm9708)] IV. C. elegans Break points: In(mak-2 unc-8 In(kvs-5 dmd-9)) IV. Covered region (Mb) 6.5 (0.7..7.2) Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30258 tmC27 [unc-75(tm9711)] I. C. elegans Break points: In(ile-1 Y18D10A.2 In(dnj-27 dkf-1)) I. Covered region (Mb) 4 (9.6..13.6) Unc. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30259 tmC29 [unc-49(tmIs1259)] III. C. elegans Break points: In(hlh-4 Y39E4.1 In(hpr-9 ttr-52)) III. Covered region (Mb) 3.7 (9.7..13.4) Balancer marked with myo-2p::GFP. Unc, semi-Emb. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30262 lin-42(tmIs1246) II. C. elegans Break points: lin-42 II. Covered region (Mb) (1.2) Balancer marked with myo-2p::Venus. Egl. [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30266 lin-42(tmIs1226) II. C. elegans Break points: lin-42 II. Covered region (Mb) (1.2) Balancer marked with myo-2p::mCherry. tmIs1226 is integrated in the same site as tmIs1246, but Egl phenotype is not detectable. [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30269 dpy-9(tm9713) kvs-5(tmIs1245) IV. C. elegans Break points: dpy-9 kvs-5 IV. Covered region (Mb) (0.3..0.7) Balancer marked with myo-2p::Venus. Dpy. [NOTE: the genotype originally listed for this strain in Table 2 of Dejima, et al. was incorrect.] Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30273 egl-17(tmIs1224) X. C. elegans Break points: egl-17 X. Covered region (Mb) (0.5) Balancer marked with myo-2p::Venus. Egl. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX30276 egl-17(tmIs1234) X. C. elegans Break points: egl-17 X. Covered region (Mb) (0.5) Balancer marked with myo-2p::mCherry. Egl. Reference: Dejima K, et al. Cell Rep. 2018 Jan 2;22(1):232-241.
FX544 cdc-48.1(tm544) II. C. elegans Received new stock 10/30/08. Attribution: This strain was generated by the National Bioresource Project at the Tokyo Women's Medical University School of Medicine, 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
FX546 sqv-5(tm546)/unc-55(e402) I. C. elegans T24D1.1 Heterozygotes are wild-type and segregate wild-type heterozygotes, unc-55 homozygotes, and sqv-5 homozygotes (sterile, clear, sickly). Attribution: This strain was generated by the National Bioresource Project at the Tokyo Women's Medical University School of Medicine, 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
FX659 cdc-48.2(tm659) II. C. elegans Received new stock 10/30/08. Attribution: This strain was generated by the National Bioresource Project at the Tokyo Women's Medical University School of Medicine, 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
FX683 spas-1(tm683) V. C. elegans Superficially WT. Attribution: This strain was generated by the National Bioresource Project at the Tokyo Women's Medical University School of Medicine, 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

Alleles contributed by this laboratory

Allele Type DNA Change Protein Change
tm1071 Allele deletion
tm1191 Allele deletion
tm1508 Allele deletion
tm2429 Allele deletion
tm1761 Allele deletion
tm1944 Allele deletion
tm668 Allele deletion
tm3039 Allele insertion
tm2886 Allele deletion
tm2214 Allele deletion
tm574 Allele deletion frameshift
tm1813 Allele deletion
tm1458 Allele insertion
tm2303 Allele deletion
tm2610 Allele deletion
tm5166 Allele deletion
tm2625 Allele insertion frameshift
tm2607 Allele insertion
tm1452 Allele insertion
tm1092 Allele deletion
tm469 Allele deletion
tm698 Allele deletion
tm805 Allele insertion
tm1133 Allele insertion
tm2443 Allele insertion
tm2144 Allele deletion
tm1791 Allele deletion
tm2713 Allele deletion
tm2181 Allele deletion
tm1325 Allele insertion
tm5503 Allele deletion
tm1684 Allele deletion
tm853 Allele insertion
tm1145 Allele deletion
tm410 Allele deletion
tm2469 Allele deletion
tm1514 Allele deletion
tm1769 Allele deletion
tm1296 Allele deletion
tm1392 Allele deletion
tm1109 Allele insertion
tm1146 Allele deletion
tm939 Allele deletion frameshift
tm2036 Allele insertion
tm246 Allele deletion
tm1524 Allele insertion
tm2066 Allele deletion
tm2355 Allele insertion
tm2394 Allele insertion
tm291 Allele deletion
tm2596 Allele deletion
tm301 Allele insertion
tm536 Allele deletion
tm546 Allele deletion
tm627 Allele deletion
tm683 Allele deletion
tm794 Allele deletion
tm863 Allele insertion
tm299 Allele deletion
tm1310 Allele deletion
tm1304 Allele deletion
tm562 Allele insertion
tm1358 Allele deletion
tm2256 Allele insertion
tm3287 Allele deletion
tm4836 Allele deletion
tm1664 Allele deletion
tm415 Allele insertion
tm514 Allele deletion
tm1652 Allele insertion
tm678 Allele deletion
tm3036 Allele deletion frameshift
tm2235 Allele deletion
tm501 Allele deletion
tm3103 Allele deletion
tm4259 Allele insertion frameshift
tm1425 Allele deletion
tm1768 Allele insertion
tm2435 Allele insertion
tm5040 Allele insertion
tm748 Allele insertion
tm483 Allele deletion
tm393 Allele deletion
tm498 Allele insertion
tm499 Allele deletion
tm2395 Allele deletion
tm1868 Allele deletion
tm1833 Allele insertion
tm2616 Allele insertion
tm329 Allele deletion
tm812 Allele insertion
tm3846 Allele deletion
tm2884 Allele deletion
tm5924 Allele deletion
tm351 Allele deletion
tm520 Allele deletion
tm1984 Allele deletion
tm2337 Allele deletion
tm597 Allele deletion
tm362 Allele deletion
tm1556 Allele deletion
tm1463 Allele deletion
tm3056 Allele deletion
tm1996 Allele deletion
tm252 Allele insertion
tm572 Allele deletion
tm761 Allele insertion
tm1689 Allele insertion
tm3681 Allele insertion
tm2432 Allele deletion
tm2810 Allele deletion
tm241 Allele deletion
tm2123 Allele insertion
tm1789 Allele deletion
tm1489 Allele deletion
tm1611 Allele deletion
tm607 Allele deletion
tm2217 Allele deletion
tm1298 Allele deletion
tm1615 Allele deletion
tm1598 Allele deletion
tm480 Allele deletion
tm3309 Allele insertion
tm472 Allele deletion
tm1099 Allele deletion
tm897 Allele insertion
tm456 Allele deletion
tm413 Allele deletion
tm801 Allele deletion
tm866 Allele deletion
tm440 Allele deletion
tm1736 Allele deletion
tm1362 Allele deletion
tm4063 Allele insertion
tm1624 Allele insertion
tm1380 Allele deletion
tm925 Allele deletion
tm2943 Allele deletion
tm1946 Allele deletion
tm1739 Allele deletion
tm3410 Allele insertion
tm3262 Allele insertion
tm442 Allele insertion
tm1692 Allele deletion
tm3647 Allele insertion
tm3395 Allele insertion
tm4567 Allele insertion
tm4263 Allele deletion
tm4795 Allele deletion
tm759 Allele deletion
tm2679 Allele deletion
tm1516 Allele deletion
tm1842 Allele deletion
tm2940 Allele insertion
tm2842 Allele deletion frameshift
tm1981 Allele deletion
tm1937 Allele deletion
tm2644 Allele deletion
tm5169 Allele deletion
tm3655 Allele deletion
tm1857 Allele insertion
tm727 Allele deletion
tm1893 Allele insertion
tm3538 Allele deletion
tm358 Allele deletion
tm324 Allele deletion
tm1411 Allele insertion
tm2050 Allele deletion
tm1307 Allele insertion
tm2590 Allele insertion
tm1037 Allele insertion
tm3024 Allele deletion
tm2047 Allele insertion
tm2720 Allele deletion
tm2820 Allele deletion
tm2921 Allele insertion
tm1753 Allele deletion
tm1909 Allele deletion
tm914 Allele deletion
tm887 Allele deletion
tm1019 Allele insertion
tm1144 Allele insertion
tm1195 Allele deletion
tm1637 Allele deletion
tm1120 Allele deletion
tm1116 Allele deletion
tm1127 Allele insertion
tm1860 Allele deletion
tm872 Allele deletion
tm1094 Allele insertion
tm1361 Allele deletion
tm892 Allele deletion
tm1155 Allele deletion
tm1227 Allele deletion
tm2182 Allele deletion frameshift
tm1661 Allele deletion
tm1579 Allele deletion
tm2484 Allele deletion frameshift
tm2868 Allele deletion
tm1724 Allele insertion
tm3256 Allele deletion
tm3827 Allele deletion