Kif5atm1.1Noh
Targeted Allele Detail
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| Symbol: |
Kif5atm1.1Noh |
| Name: |
kinesin family member 5A; targeted mutation 1.1, Nobutaka Hirokawa |
| MGI ID: |
MGI:5495649 |
| Gene: |
Kif5a Location: Chr10:127061565-127099217 bp, - strand Genetic Position: Chr10, 74.5 cM
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| Alliance: |
Kif5atm1.1Noh page
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| Germline Transmission: |
Earliest citation of germline transmission:
J:197666
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| Parent Cell Line: |
CMTI-1 (ES Cell)
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| Strain of Origin: |
129S6/SvEvTac
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| Allele Type: |
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Targeted (Null/knockout) |
| Mutations: |
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Insertion, Intragenic deletion
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Mutation details: A floxed beta-geo (neomycin resistance and lacZ) cassette was inserted upstream of exon 2. An additional loxP site was inserted downstream of exon 4. Cre-mediated recombination removed exons 2 through 4 and the beta-geo cassette. Western blot analysis confirmed the absence of protein expression in the brain.
(J:197666)
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View phenotypes and curated references for all genotypes (concatenated display).
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| Mouse strains and cell lines
available from the International Mouse Strain Resource
(IMSR) |
| Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available
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| Carrying any Kif5a Mutation: |
55 strains or lines available
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| Original: |
J:197666 Nakajima K, et al., Molecular motor KIF5A is essential for GABA(A) receptor transport, and KIF5A deletion causes epilepsy. Neuron. 2012 Dec 6;76(5):945-61 |
| All: |
1 reference(s) |
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