Nrxn1em1Joez
Endonuclease-mediated Allele Detail
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| Symbol: |
Nrxn1em1Joez |
| Name: |
neurexin I; endonuclease-mediated mutation 1, Zhaolan Zhou |
| MGI ID: |
MGI:7449236 |
| Synonyms: |
Nrxn1deltaIntron17 |
| Gene: |
Nrxn1 Location: Chr17:90341059-91400499 bp, - strand Genetic Position: Chr17, 59.73 cM
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| Alliance: |
Nrxn1em1Joez page
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| Strain of Origin: |
C57BL/6J x SJL
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| Allele Type: |
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Endonuclease-mediated (Not Applicable) |
| Mutation: |
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Intragenic deletion
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Mutation details: CRISPR/Cas9 technology using sgRNAs 5 AATATGTGGGCAAGCTGGGTTGG 3 AND 5GAAATGGTACCTTTGATTAAGG 3 generated an approximate 20 kb deletion at intron 17. This is similar to a deletion identified in an individual on the autism spectrum. Both Nrxn1alpha and Nrxn1gamma transcript levels are unaffected while Nrxn1beta levels are slightly reduced in homozygous males but not in females.
(J:334083)
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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 Nrxn1 Mutation: |
102 strains or lines available
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| Original: |
J:334083 Xu B, et al., Allelic contribution of Nrxn1alpha to autism-relevant behavioral phenotypes in mice. PLoS Genet. 2023 Feb;19(2):e1010659 |
| All: |
1 reference(s) |
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