Strain Information | |
---|---|
Image | |
BRC No. | RBRC10352 |
Type | CRISPR/Cas9 (Transgene)![]() |
Species | Mus musculus |
Strain name | STOCK Llcfc1<em2Osb> |
Former Common name | 1700034O15Rik (Llcfc1)<-1024/wt>, SOF1 |
H-2 Haplotype | |
ES Cell line | EGR-G01 [129S2 x C57BL/6NCr-Tg(CAG/Acr-EGFP)] |
Background strain | |
Appearance | |
Strain development | Developed by Taichi Noda and Masahito Ikawa, Research Institute for Microbial Diseases, Osaka University in 2017. EGR-G01 ES cells derived from (129S2 x B6Cr)F1 were used. Mice were crossed with B6D2F1. Mixed genetic background. Homozygous males are infertile. |
Strain description | Llcfc1<em2Osb>; 1024 bp deletion at exon 1aagctccaatggaggttactgctatgcatactgatgcctgtcatcttgtgtgggagatgtgtttttccagtgacttctcatctaagtagtgactatgagaatattgttgcattagagtataggtagctatgcagatccaacagtgtaatagatatgatacttagcaacttttggaacccttttaggttgtggtatataaggtgatccattatgaccatctcagatgcctctgccatctcccacccttctgtctggcaatggaatggtataaagatCTAGAATGTAGGATATAGCCATGGCAGCGATGTCATAGGACACATAGAATCAGAGGTCCTATGGAAGAGAAGGAGGAAAAGCGATGCTGTCAAGGGGTAAGAGCTAAGAAAGGGATGGGGTGGTGTTGGTAGCTGGGGATTGGGGCCAAAGGAAGCATGGGAGAGGAGACCCATGACTTCTCTGGGCTCCCAGCTCCACAGAGCAACATTCCTGACAGCTTTGTTGCTACTGCTGCTGCTCCAAGTGAAGGGGGTGAAGACTCTGATAGTGAGTGCAAGCTTGGATGGTGACAAGAGTCAGAAAGACAAAGTGTCCTCTGAAGgtgggtagaggagagaggtagaggatggatggtgggggaggggtgctggacataagggttttcttggattcacatcaggctccagcagcagactaggtcatggttaatatggggtttgaattttggcagataactcatgttccctatcaccatagcatgaaataatagctgtaggtaaaattgtttagttttacaaagtctcttagccaggtcacagaatggggctacctacagttgtcaaaggcttctgaggaagtagagtgcctaaagagggcctctttgccttcatgtttgaagttatctctcactcctttggaggagggaactagagtaagacatggttatcacctgtgtttgagatggggctatggttgaagtgagacttgaaaagccctctagataaagcattctctcactgcgtcaaggccagtgttatgactggcagtagttacgacttatctctcaaccgttcccctcctcccctttctgataaagaatagaagttcgactggagctgcccatctctgcccttcttttatgttgtagACCAGGGTGAGGAGGAGTATGAAGAACACTTTGAGGCTTCATCAGAGGGTGAGCAGTGGCAGGAGATAGATATGGTCCAGCAAGAAGACACGATCTCCCAGGCAATAACTCTCCAGGACCACCTCCTTGACCTAGCCTTCTGCTTCAACCTGGCCAGCATCATGTTTTTTTTATGAGAGACTTTGAGGTGGAGGCAGTAGTCTGGATCCTTCATGAGGACTTAGACATCCACCTCCCCTTCCTGATTGCTTACTGACCTCCTCTCCTAAATGCCTCCTCAAAATGCACACCCTGGTCCCTGTCTCTAAGAAGTACCTGACCTTAGGGTATATCAACAGAGCTTTCCCAACTCTCATATCCACCACCTAATTGCCACCCCAACCCAGAATTTCATGTCCCG |
Colony maintenance | |
References | Sperm proteins SOF1, TMEM95, and SPACA6 are required for sperm-oocyte fusion in mice. Noda T, Lu Y, Fujihara Y, Oura S, Koyano T, Kobayashi S, Matzuk M M, Ikawa M Proc. Natl. Acad. Sci. USA, 117(21):11493-11502 (2020). 32393636ZP2 cleavage blocks polyspermy by modulating the architecture of the egg coat. Shunsuke Nishio, Chihiro Emori, Benjamin Wiseman, Dirk Fahrenkamp, Elisa Dioguardi, Sara Zamora-Caballero, Marcel Bokhove, Ling Han, Alena Stsiapanava, Blanca Algarra, Yonggang Lu, Mayo Kodani, Rachel E Bainbridge, Kayla M Komondor, Anne E Carlson, Michael Landreh, Daniele de Sanctis, Shigeki Yasumasu, Masahito Ikawa, Luca Jovine Cell, 187(6):1440-1459.e24 (2024). 38490181 |
Health Report | |
---|---|
Examination Date / Room / Rack |
Gene | |||||||
---|---|---|---|---|---|---|---|
Gene Symbol | Gene Name | Chr. | Allele Symbol | Allele Name | Common Names | Promoter | Diseases Related to This Gene |
Llcfc1 MGI:1923856 | LLLL and CFNLAS motif containing 1 | 6 | Llcfc1<em2Osb> MGI:6437831 | endonuclease-mediated mutation 2, Research Institute for Microbial Diseases, Osaka University |
Phenotype | |
---|---|
Annotation by Mammalian phenotyhpe ontology | |
Detailed phenotype data |
Ordering Information | |
---|---|
Donor DNA | pX330-U6-Chimeric_BB-CBh-hSpCas9[human U6 promoter, S. pyogenes gRNA scaffold, human U6 terminator, CMV,chicken hybrid CMV enhancer/chicken beta-actin promoter (CBh), Synthetic DNA 3xFLAG, SV40 nuclear localization signal(NLS), Streptococcus pyogenes SpCas9 (human codon-optimized), bovine GH polyA signal, AAV2 inverted terminal repeat (ITR), f1 phage f1 origin, E. coli Ampicillin resistance gene (AmpR), E. coli pUC origin], Mouse a part of Llcfc1 gene |
Research application | |
Specific Term and Conditions | The RECIPIENT of BIOLOGICAL RESOURCE shall obtain a prior written consent on use of it from the DEPOSITOR. In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of the following literature(s) designated by the DEPOSITOR is requested. Proc. Natl. Acad. Sci. USA, 117(21):11493-11502 (2020).The RECIPIENT of BIOLOGICAL RESOURCE shall obtain a prior written consent on use of it from the DEPOSITOR. RECIPIENT which wants to use the BIOLOGICAL RESOURCE for the purpose other than education or not-for-profit research is requested to enter into a Material Transfer Agreement with Osaka University. In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of the following literature(s) designated by the DEPOSITOR is requested. The RECIPIENT which wants to use the BIOLOGICAL RESOURCE even after five years must obtain a written consent from the DEPOSITOR again. |
Depositor | Masahito Ikawa (Osaka University) |
Strain Status | ![]() |
Strain Availability | ![]() |
Additional Info. | Necessary documents for ordering:
|
BRC mice in Publications |
---|
No Data |