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Unc13atm1Bros
Targeted Allele Detail
Summary
Symbol: Unc13atm1Bros
Name: unc-13 homolog A; targeted mutation 1, Nils Brose
MGI ID: MGI:2449468
Synonyms: Munc13-1-deficient, Unc13aKO
Gene: Unc13a  Location: Chr8:72079356-72124418 bp, - strand  Genetic Position: Chr8, 34.43 cM, cytoband B3.3
Alliance: Unc13atm1Bros page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:56513
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsThe gene was disrupted by the replacement of 4 exons encoding amino acids 494-619 (which includes the C1 domain) with a neomycin resistance cassette via homologous recombination. The null allele was confirmed by Western blot analysis using antibodies directed against the extreme N- and C-termini of the protein. (J:56513)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 5 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Unc13a Mutation:  74 strains or lines available
References
Original:  J:56513 Augustin I, et al., Munc13-1 is essential for fusion competence of glutamatergic synaptic vesicles. Nature. 1999 Jul 29;400(6743):457-61
All:  35 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory