- belly spot / MGI
- impaired hearing / MGI
- increased or absent threshold for auditory brainstem response / MGI
- abnormal inner ear morphology / MGI
- absent semicircular canals / MGI
- short tail / MGI
- hyperactivity / MGI
- impaired righting response / MGI
- abnormal placing response / MGI
- deafness / MGI
- absent otoliths / MGI
- abnormal cochlear inner hair cell morphology / MGI
- abnormal vestibular labyrinth morphology / MGI
- head tossing / MGI
- dilated endolymphatic duct / MGI
- dilated endolymphatic sac / MGI
- abnormal otic vesicle development / MGI
- abnormal vestibular saccule morphology / MGI
- abnormal utricle morphology / MGI
- absent pinna reflex / MGI
- short scala media / MGI
STOCK Lmx1amtl/Cnbc
Status | Available to order |
EMMA ID | EM:04898 |
Citation information | RRID:IMSR_EM:04898 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 | STOCK Lmx1amtl/Cnbc |
Alternative name | Mutanlallemande |
Strain type | Spontaneous |
Allele/Transgene symbol | Lmx1amtl |
Gene/Transgene symbol | Lmx1a |
Information from provider
Provider | Karen Steel |
Provider affiliation | Wellcome Trust Sanger Institute |
Additional owner | Yvan Lallemand and Jean-Louis Guenet, Institut Pasteur, discovered the mutant. |
Genetic information | A spontaneous mutation of Lmx1a. |
Phenotypic information | Homozygotes show severe head bobbing and circling, white belly spot or belt and are small. |
Breeding history | The mutant was introduced on a mixed genetic background and has been maintained within a closed colony for over ten years. |
References | None available |
Homozygous fertile | no |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | not known |
Information from EMMA
Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Disease and phenotype information
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal inner ear morphology / MGI
- abnormal cochlea morphology / MGI
- abnormal inner ear vestibule morphology / MGI
- abnormal membranous labyrinth morphology / MGI
- absent semicircular canals / MGI
- abnormal interparietal bone morphology / MGI
- abnormal parietal bone morphology / MGI
- abnormal cell proliferation / MGI
- belly spot / MGI
- synostosis / MGI
- kinked tail / MGI
- short tail / MGI
- decreased brain size / MGI
- abnormal hippocampus development / MGI
- abnormal cerebellum morphology / MGI
- small cerebellum / MGI
- abnormal cerebellum development / MGI
- abnormal cerebellar foliation / MGI
- abnormal cerebellum posterior vermis morphology / MGI
- abnormal roof plate morphology / MGI
- abnormal rhombomere morphology / MGI
- abnormal glossopharyngeal nerve morphology / MGI
- abnormal glossopharyngeal ganglion morphology / MGI
- uterus hypoplasia / MGI
- decreased body size / MGI
- ataxia / MGI
- circling / MGI
- bidirectional circling / MGI
- hyperactivity / MGI
- abnormal motor coordination/balance / MGI
- impaired righting response / MGI
- abnormal placing response / MGI
- hydroencephaly / MGI
- infertility / MGI
- male infertility / MGI
- female infertility / MGI
- deafness / MGI
- postnatal lethality / MGI
- premature death / MGI
- abnormal neural tube morphology / MGI
- abnormal fertility/fecundity / MGI
- abnormal semicircular canal morphology / MGI
- belted / MGI
- altered righting response / MGI
- white spotting / MGI
- absent otoliths / MGI
- no phenotypic analysis / MGI
- spina bifida / MGI
- abnormal cell migration / MGI
- abnormal ear development / MGI
- abnormal bony labyrinth / MGI
- absent vestibular saccule / MGI
- absent utricle / MGI
- abnormal cochlear inner hair cell morphology / MGI
- abnormal cochlear labyrinth morphology / MGI
- abnormal vestibular labyrinth morphology / MGI
- syndromic hearing loss / MGI
- abnormal vertebral arch development / MGI
- head tossing / MGI
- abnormal cell physiology / MGI
- dilated endolymphatic duct / MGI
- dilated endolymphatic sac / MGI
- abnormal otic vesicle development / MGI
- abnormal vestibular saccule morphology / MGI
- abnormal utricle morphology / MGI
- abnormal tail development / MGI
- inner ear hypoplasia / MGI
- impaired hearing / MGI
- absent pinna reflex / MGI
- abnormal hippocampus CA3 region morphology / MGI
- abnormal hippocampus pyramidal cell layer / MGI
- short scala media / MGI
- bleb / MGI
- abnormal resting posture / MGI
- reduced cerebellar foliation / MGI
- abnormal neuron differentiation / MGI
- mortality/aging / MGI
- prenatal lethality, complete penetrance / MGI
- preweaning lethality, incomplete penetrance / MGI
- decreased dopaminergic neuron number / MGI
- increased or absent threshold for auditory brainstem response / MGI
- abnormal rhombomere 3 morphology / MGI
- abnormal rhombomere 4 morphology / MGI
- abnormal rhombomere 5 morphology / MGI
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