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Strain: SD-Fmr1em1Sage

Symbol: SD-Fmr1em1Sage
Strain: SD-Fmr1em1
Substrain: Sage
RGD ID: 11568040
Citation ID: RRID:RGD_11568040
Ontology ID: RS:0004275
Alleles: Fmr1em1Sage
Also Known As: TGRS5390; SD- Fmr1 tm1sage; SD-Fmr1em1Sage; Fmr1-Δexon 8 rat; SD-Fmr1^[em1Sage]
Type: mutant
Available Source: Horizon Discovery
Origination: Horizon Discovery
Description: The ZFN mutant rat strain was produced by injecting zinc finger nuclease targeting rat Fmr1 into Sprague Dawley embryos. The resulting mutation was a 122bp deletion of the intron 7/exon8 junction occurred at 18533bp-18654bp. This mutant rat has a knockout of Fmr1.
Genetic Status: Homozygous
Last Known Status: Live Animals (as of 2017-05-09)
Research Usage Autism, Fragile X syndrome
Position
Rat AssemblyChrPosition (strand)SourceJBrowse
GRCr8X152,284,857 - 152,322,686RGD_MAPPER_PIPELINE
mRatBN7.2X147,258,833 - 147,258,954RGD_MAPPER_PIPELINEmRatBN7.2
Rnor_6.0X154,703,661 - 154,703,782RGD_MAPPER_PIPELINERnor6.0
RGSC_v3.4X154,756,031 - 154,793,782RGD_MAPPER_PIPELINERGSC3.4





References

References - curated
# Reference Title Reference Citation
1. Experience-dependent changes in hippocampal spatial activity and hippocampal circuit function are disrupted in a rat model of Fragile X Syndrome. Asiminas A, etal., Mol Autism. 2022 Dec 20;13(1):49. doi: 10.1186/s13229-022-00528-z.
2. Auditory hypersensitivity and processing deficits in a rat model of fragile X syndrome. Auerbach BD, etal., Neurobiol Dis. 2021 Dec;161:105541. doi: 10.1016/j.nbd.2021.105541. Epub 2021 Oct 29.
3. Sensory hypo-excitability in a rat model of fetal development in Fragile X Syndrome. Berzhanskaya J, etal., Sci Rep. 2016 Jul 28;6:30769. doi: 10.1038/srep30769.
4. FMR1 deletion in rats induces hyperactivity with no changes in striatal dopamine transporter availability. D'Elia A, etal., Sci Rep. 2022 Dec 29;12(1):22535. doi: 10.1038/s41598-022-26986-2.
5. Deletion of the KH1 Domain of Fmr1 Leads to Transcriptional Alterations and Attentional Deficits in Rats. Golden CEM, etal., Cereb Cortex. 2019 May 1;29(5):2228-2244. doi: 10.1093/cercor/bhz029.
6. Fmr1 and Nlgn3 knockout rats: novel tools for investigating autism spectrum disorders. Hamilton SM, etal., Behav Neurosci. 2014 Apr;128(2):103-9. doi: 10.1037/a0035988.
7. Brain Cholesterol Biosynthetic Pathway Is Altered in a Preclinical Model of Fragile X Syndrome. Parente M, etal., Int J Mol Sci. 2022 Mar 21;23(6):3408. doi: 10.3390/ijms23063408.
8. Abnormal neuronal morphology and neurochemistry in the auditory brainstem of Fmr1 knockout rats. Ruby K, etal., Neuroscience. 2015 Sep 10;303:285-98. doi: 10.1016/j.neuroscience.2015.06.061. Epub 2015 Jul 9.

Region

Allelic Variants
Name Chromosome Start Pos End Pos Reference Nucleotide Variant Nucleotide Variant Type Assembly
Fmr1em1Sage-var1 chrX 147258833 147258954 CATGGCTGGCCTAAATGAAATTGACTTAATAATTGGTAAAACAAGTTAATCACTTGTGCATTTCTCTTCAGAGTTCAAGGCAGCTTGCCTCAAGATTTCATGAACAGTTTATCGTACGAGAA - deletion mRatBN7.2
Fmr1em1Sage-var1 chrX 154703661 154703782 CATGGCTGGCCTAAATGAAATTGACTTAATAATTGGTAAAACAAGTTAATCACTTGTGCATTTCTCTTCAGAGTTCAAGGCAGCTTGCCTCAAGATTTCATGAACAGTTTATCGTACGAGAA - deletion Rnor_6.0

Additional Information