Del(7Coro1a-Spn)1Dolm
Targeted Allele Detail
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Symbol: |
Del(7Coro1a-Spn)1Dolm |
Name: |
deletion, Chr 7, Ricardo Dolmetsch 1 |
MGI ID: |
MGI:5569506 |
Synonyms: |
16p11-, 16p11.2 |
Gene: |
Del(7Coro1a-Spn)1Dolm Location: unknown Genetic Position: Chr7, Syntenic
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Germline Transmission: |
Earliest citation of germline transmission:
J:210018
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Parent Cell Line: |
Not Specified (ES Cell)
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Strain of Origin: |
129P2/OlaHsd
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Allele Type: |
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Targeted (Null/knockout, Reporter) |
Mutations: |
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Intergenic deletion, Intragenic deletion
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Del(7Coro1a-Spn)1Dolm involves 39 genes/genome features (Gm25333, Gm15676, Coro1a ...)
View all
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Mutation details: Two sequential targeting events generated Igs14tm1Dolm and Igs13tm1Dolm. Cre-mediated recombination removed both floxed neomycin cassettes creating a deletion that spans 440 kbp region on mouse chromosome 7F3 (between and including Coro1a to Spn); a region highly conserved with the human chromosome 16p11.2 region whose copy number variations are associated with autism spectrum disorders and schizophrenia.
(J:210018)
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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: 1 strain available
Cell Lines: 0 lines available
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Carrying any Del(7Coro1a-Spn)1Dolm Mutation: |
1 strain or line available
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Original: |
J:210018 Portmann T, et al., Behavioral abnormalities and circuit defects in the Basal Ganglia of a mouse model of 16p11.2 deletion syndrome. Cell Rep. 2014 May 22;7(4):1077-92 |
All: |
1 reference(s) |
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