Strain Information | |
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Image | |
BRC No. | RBRC06218 |
Type | Targeted Mutation![]() |
Species | Mus musculus |
Strain name | C57BL/6-Susd3<tm1(KOMP)Vlcg> |
Former Common name | Susd3 KO, B6-Susd3 KO |
H-2 Haplotype | |
ES Cell line | VGB6 [C57BL/6NTac] |
Background strain | C57BL/6NTac |
Appearance | |
Strain development | Developed by Yoshihiro Omori and Takahisa Furukawa, Institute for Protein Research, Osaka University. The original allele and mouse were on C57BL/6 background and from the Knockout Mouse Project (KOMP) Repository. |
Strain description | Susd3, sushi domain containing 3 gene knockout mice. A 17004 bp region between 49,343,498-49,326,495 positions of Chromosome 13 was deleted by the insertion of ZEN-Ub1 cassette. Homozygous mutant mice are viable and fertile. |
Colony maintenance | Homozygote x Homozygote [or Crossing to C57BL/6NTac] |
References |
Health Report | |
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Examination Date / Room / Rack |
Gene | |||||||
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Gene Symbol | Gene Name | Chr. | Allele Symbol | Allele Name | Common Names | Promoter | Diseases Related to This Gene |
Pgk1 | mouse PGK polyA signal | 13 | Pgk1 | ||||
Susd3 MGI:1913579 | sushi domain containing 3 | 13 | Susd3<tm1(KOMP)Vlcg> MGI:5292886 | targeted mutation 1, Velocigene | |||
lacZ | beta-galactosidase (E. coli) | 13 | |||||
loxP | phage P1 loxP | 13 | loxP | ||||
loxP | phage P1 loxP | 13 | loxP | ||||
neo | neomycin resistance gene (E. coli) | 13 | human ubiquitin C promoter | ||||
SV40 polyA signal | 13 |
Phenotype | |
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Annotation by Mammalian phenotyhpe ontology | |
Detailed phenotype data |
Ordering Information | |
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Donor DNA | Velocigene cassette ZEN-Ub1(E. coli Beta-galactosidase, SV40 polyA, phage P1 loxP sites, human ubiquitin C promoter, E. coli neoR gene, mouse PGK polyA), mouse Susd3 genomic DNA |
Research application | Cell Biology Research Cre/loxP system Fluorescent Proteins/lacZ System |
Specific Term and Conditions | The use of the BIOLOGICAL RESOURCE is strictly limited to academic, non-profit research institutes for academic non-profit research purposes. Prior to requesting the BIOLOGICAL RESOURCE, the RECIPIENT must contract an MTA with the DEPOSITOR (Osaka University). In publishing the research results to be obtained by use of the BIOLOGICAL RESOURCE, an acknowledgment to the DEPOSITOR and a mention of the Knockout Mouse Project and the KOMP Repository as the source of the original allele and mice are requested. |
Depositor | Takahisa Furukawa (Osaka University) |
Strain Status | ![]() |
Strain Availability | Recovered litters from cryopreserved sperm (2 to 4 months) Cryopreserved sperm (within 1 month) |
Additional Info. | Necessary documents for ordering:
Genotyping protocol -PCR- |
BRC mice in Publications |
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No Data |