- abnormal cochlea morphology / MGI
- abnormal lateral semicircular canal morphology / MGI
- delayed bone ossification / MGI
- abnormal hair follicle morphology / MGI
- decreased hair follicle number / MGI
- small hair follicles / MGI
- abnormal liver morphology / MGI
- muscle hypoplasia / MGI
- decreased oligodendrocyte progenitor number / MGI
- abnormal spinal cord morphology / MGI
- atelectasis / MGI
- translucent skin / MGI
- thin epidermis / MGI
- thin epidermis stratum spinosum / MGI
- decreased body weight / MGI
- cyanosis / MGI
- postnatal growth retardation / MGI
- respiratory failure / MGI
- abnormal postnatal growth/weight/body size / MGI
- abnormal muscle morphology / MGI
- hydrops fetalis / MGI
- abnormal semicircular canal morphology / MGI
- abnormal posterior semicircular canal morphology / MGI
- abnormal cochlear sensory epithelium morphology / MGI
- abnormal bony labyrinth / MGI
- abnormal cochlear inner hair cell morphology / MGI
- decreased cochlear inner hair cell number / MGI
- abnormal cochlear outer hair cell morphology / MGI
- decreased cochlear outer hair cell number / MGI
- decreased cochlear hair cell number / MGI
- abnormal cochlear hair cell stereociliary bundle morphology / MGI
- abnormal cochlear hair cell development / MGI
- abnormal brainstem morphology / MGI
- homeostasis/metabolism phenotype / MGI
- growth/size/body region phenotype / MGI
- decreased birth weight / MGI
- prenatal growth retardation / MGI
- abnormal inner hair cell kinocilium morphology / MGI
- neonatal lethality, complete penetrance / MGI
B6;129S5-Igf1rtm1Lex/Ieg
Status | Available to order |
EMMA ID | EM:02317 |
International strain name | B6;129S5-Igf1rtm1Lex/Ieg |
Alternative name | LEXKO-322, MEM490C1 |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Igf1rtm1Lex |
Gene/Transgene symbol | Igf1r |
Information from provider
Provider | Lexicon Genetics, Inc. |
Provider affiliation | Lexicon Pharmaceuticals |
Phenotypic information | Genetic data indicate that this mutation resulted in lethality of the homozygous mutants. No notable phenotype was observed for the heterozygous mice. Disruption of the target gene was confirmed by Southern hybridization analysis. |
References | None available |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Growth delay due to insulin-like growth factor I resistance / Orphanet_73273
MGI phenotypes (gene matching)
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