Ephb3tm1.1Meg
Targeted Allele Detail
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| Symbol: |
Ephb3tm1.1Meg |
| Name: |
Eph receptor B3; targeted mutation 1.1, Michael E Greenberg |
| MGI ID: |
MGI:5505688 |
| Synonyms: |
EphB3T706A |
| Gene: |
Ephb3 Location: Chr16:21023530-21042054 bp, + strand Genetic Position: Chr16, 12.62 cM, cytoband B1-B4
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| Alliance: |
Ephb3tm1.1Meg page
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| Germline Transmission: |
Earliest citation of germline transmission:
J:197489
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| Parent Cell Line: |
J1 (ES Cell)
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| Strain of Origin: |
129S4/SvJae
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| Allele Type: |
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Targeted |
| Mutation: |
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Single point mutation
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Mutation details: A point mtuation (A to G) in exon 11 results in the amino acid substitution of threonine with alanine at position 706 (p.T706A) in the encoded protein. This mutation creates a PP1 analog-sensitive protein. Cre-mediated recombination removed the loxP site flanked neomycin resistance gene cassette inserted into intron 9.
(J:197489)
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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 Ephb3 Mutation: |
54 strains or lines available
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| Original: |
J:197489 Soskis MJ, et al., A chemical genetic approach reveals distinct EphB signaling mechanisms during brain development. Nat Neurosci. 2012 Dec;15(12):1645-54 |
| All: |
2 reference(s) |
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