ObscnMSN/GammMmmh
Spontaneous Allele Detail
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Symbol: |
ObscnMSN/GammMmmh |
Name: |
obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF; MSN/GammMmmh |
MGI ID: |
MGI:6471803 |
Synonyms: |
ObscnV1583PV V6941M H586Y |
Gene: |
Obscn Location: Chr11:58885082-59027201 bp, - strand Genetic Position: Chr11, 36.4 cM
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Alliance: |
ObscnMSN/GammMmmh page
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Allele Type: |
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Spontaneous |
Mutations: |
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Insertion, Single point mutation
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Mutation details: This allele contains the following spontaneous mutation(s) that have a predicted consequential effect on the encoded peptide and that are specific to (fixed in) the MSN (Madison) strain used as a mania model, as compared to: the Hsd:ICR strain from which it is derived; the MaD2 (Maternal Defense 2) strain, which is also derived from Hsd:ICR but wasn't selected for mania; the C57BL/6J reference strain. Build GRCm38 genomic coordinates: g.chr11:59000521C>CTGG (p.P7061dup); g.chr11:59000884C>T (p.V6941M); g.chr11:59076137G>A (p.H3164Y).
(J:267654)
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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 Obscn Mutation: |
420 strains or lines available
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Original: |
J:267654 Saul MC, et al., Genomic variants in an inbred mouse model predict mania-like behaviors. PLoS One. 2018;13(5):e0197624 |
All: |
1 reference(s) |
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