Slc1a4em1Tmg
Endonuclease-mediated Allele Detail
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| Symbol: |
Slc1a4em1Tmg |
| Name: |
solute carrier family 1 (glutamate/neutral amino acid transporter), member 4; endonuclease-mediated mutation 1, Teresa M Gunn |
| MGI ID: |
MGI:7574170 |
| Gene: |
Slc1a4 Location: Chr11:20252180-20282713 bp, - strand Genetic Position: Chr11, 12.97 cM
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| Alliance: |
Slc1a4em1Tmg page
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| Allele Type: |
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Endonuclease-mediated (Null/knockout) |
| Mutation: |
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Intragenic deletion
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Mutation details: CRISPR/Cas9 technology generated a 10-bp deletion in exon 4 that results in a frameshift and premature stop codon. Western blot analysis confirmed the absence of protein in brain lysates.
(J:344184)
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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 Slc1a4 Mutation: |
41 strains or lines available
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| Original: |
J:344184 Ratz-Mitchem ML, et al., Generation and characterization of a knock-in mouse model for spastic tetraplegia, thin corpus callosum, and progressive microcephaly (SPATCCM). Mamm Genome. 2023 Dec;34(4):572-585 |
| All: |
1 reference(s) |
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