- enlarged lymph nodes / IMPC
- abnormal auditory brainstem response / IMPC
- abnormal colon morphology / IMPC
- decreased prepulse inhibition / IMPC
- decreased startle reflex / IMPC
- decreased exploration in new environment / IMPC
- abnormal lymph node morphology / IMPC
- abnormal adrenal gland morphology / IMPC
- abnormal uterus morphology / IMPC
- abnormal eye morphology / IMPC
- enlarged uterus / IMPC
- cataract / IMPC
- abnormal kidney morphology / IMPC
- abnormal startle reflex / IMPC
C57BL/6N-Slc17a8tm2Selm/Ics
| Status | Available to order |
| EMMA ID | EM:05733 |
| Citation information | RRID:IMSR_EM:05733 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
| International strain name | C57BL/6N-Slc17a8tm2Selm/Ics |
| Alternative name | VGluT3cKO |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Slc17a8tm2Selm |
| Gene/Transgene symbol | Slc17a8 |
Information from provider
| Provider | Salah El Mestikawy |
| Provider affiliation | U952 INSERM CNRS UMR7224, Université Paris 6, PMSNC |
| Genetic information | Two loxP sites have been inserted around exon2 of the Slc17a8 (Vglut3) gene. |
| Phenotypic information | Not characterised. |
| Breeding history | This line was created on C57BL/6N background and maintained on this same background. |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
| Animals used for archiving | heterozygous C57BL/6NTac males, wild-type C57BL/6NTac females |
| Stage of embryos | 8-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal dominant non-syndromic sensorineural deafness type DFNA / Orphanet_90635
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- nonconvulsive seizures / MGI
- hyperactivity / MGI
- deafness / MGI
- abnormal cochlear ganglion morphology / MGI
- cochlear ganglion degeneration / MGI
- abnormal neurotransmitter uptake / MGI
- decreased cochlear inner hair cell number / MGI
- absent cochlear nerve compound action potential / MGI
- abnormal cochlear inner hair cell physiology / MGI
- decreased synaptic glutamate release / MGI
- abnormal inner hair cell synaptic ribbon morphology / MGI
- abnormal cochlear IHC efferent innervation pattern / MGI
- abnormal auditory brainstem response / MGI
- sensorineural hearing loss / MGI
- abnormal synaptic acetylcholine release / MGI
- abnormal brain wave pattern / MGI
- hearing/vestibular/ear phenotype / MGI
- absent startle reflex / MGI
- impaired behavioral response to xenobiotic / MGI
- enhanced behavioral response to cocaine / MGI
- increased or absent threshold for auditory brainstem response / MGI
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