Laboratory Information
| Name | FX View on WormBase |
|---|---|
| Allele designation | tm |
| Head | Shohei Mitani |
| Institution | Tokyo 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 WT and 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) III; 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). Pick wild-type to maintain. Heterozygotes are wild-type and segregate wild-type heterozygotes, Dpy (tmIn14 homozygotes), and unc-15 homozygotes. [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) III; 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 I; lig-4(tm750) III. | 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. |
| 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 | tmIs1240 [myo-2p::Venus, X: F23D12.4] X. tmEx4950 [unc-9(+) + vha-6p::GFP]. Pick non-Unc with bright GFP+ in gut to maintain array. Balancer marked with myo-2p::Venus. Mec (Unc). Balancer break points: In(mec-10 Y7A5A.20 In(odr-7 F59F4.2)) X. Covered region (Mb) 7.4 (8.5..15.8) 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 | tmIs1233 [myo-2p::mCherry, X: F23D12.4] X. tmEx4950 [unc-9(+) + vha-6p::GFP]. Pick non-Unc with bright GFP+ in gut to maintain array. Balancer marked with myo-2p::mCherry. Mec (Unc). Balancer break points: In(mec-10 Y7A5A.20 In(odr-7 F59F4.2)) X. Covered region (Mb) 7.4 (8.5..15.8) 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. |
| 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 |