- increased mean platelet volume / IMPC
- persistence of hyaloid vascular system / IMPC
- hyperactivity / IMPC
- decreased circulating serum albumin level / IMPC
- impaired righting response / IMPC
- abnormal vertebrae morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
- increased circulating aspartate transaminase level / IMPC
B6;129-Klf7tm1Rmz/Cnrm
Status | Available to order |
EMMA ID | EM:04785 |
Citation information | RRID:IMSR_EM:04785 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 | B6;129-Klf7tm1Rmz/Cnrm |
Alternative name | Klf7 +/- |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Klf7tm1Rmz |
Gene/Transgene symbol | Klf7 |
Information from provider
Provider | Francesco Ramirez |
Provider affiliation | Department of Pharmacology and Systems Therapeutics, Mount Sinai School of Medicine |
Additional owner | Prof. Bruce Krueger, University of Maryland School of Medicine, Baltimore MD, U.S.A. |
Genetic information | The targeting vector was designed to replace most of exon 1 with the phosphoglycerate kinase (PGK)-neo cassette flanked by loxP sites. |
Phenotypic information | Klf7 +/- mice display no anatomical abnormalities and are fertile and viable. Klf7 knock-out mice die within 3 days after birth, displaying severely hypoplastic olfactory bulbs, and altered neuronal differentiation in the central nervous system. |
Breeding history | The strain was inbred for 4 generations. It is currently bred using Klf7 +/- males and wild-type females. |
References |
|
Homozygous fertile | no |
Homozygous viable | no |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (allele matching)
- abnormal nervous system tract morphology / MGI
- abnormal corpus callosum morphology / MGI
- abnormal telencephalon morphology / MGI
- abnormal cerebral cortex morphology / MGI
- abnormal dentate gyrus morphology / MGI
- abnormal sensory neuron innervation pattern / MGI
- unresponsive to tactile stimuli / MGI
- cyanosis / MGI
- hypopnea / MGI
- abnormal brain morphology / MGI
- small olfactory bulb / MGI
- abnormal axon guidance / MGI
- abnormal hippocampal fimbria morphology / MGI
- abnormal axon extension / MGI
- abnormal olfactory nerve morphology / MGI
- absent anterior commissure / MGI
- absent gastric milk in neonates / MGI
- abnormal hippocampus pyramidal cell morphology / MGI
- postnatal lethality, complete penetrance / MGI
- abnormal olfactory neuron innervation pattern / MGI
MGI phenotypes (gene matching)
- abnormal nervous system tract morphology / MGI
- abnormal corpus callosum morphology / MGI
- abnormal telencephalon morphology / MGI
- abnormal cerebral cortex morphology / MGI
- abnormal dentate gyrus morphology / MGI
- abnormal sensory neuron innervation pattern / MGI
- unresponsive to tactile stimuli / MGI
- cyanosis / MGI
- hypopnea / MGI
- abnormal brain morphology / MGI
- small olfactory bulb / MGI
- abnormal axon guidance / MGI
- abnormal hippocampal fimbria morphology / MGI
- abnormal axon extension / MGI
- abnormal olfactory nerve morphology / MGI
- absent anterior commissure / MGI
- absent gastric milk in neonates / MGI
- abnormal hippocampus pyramidal cell morphology / MGI
- postnatal lethality, complete penetrance / MGI
- abnormal olfactory neuron innervation pattern / MGI
Literature references
- Transcription factor KLF7 is important for neuronal morphogenesis in selected regions of the nervous system.;Laub Friedrich, Lei Lei, Sumiyoshi Hideaki, Kajimura Daisuke, Dragomir Cecilia, Smaldone Silvia, Puche Adam C, Petros Timothy J, Mason Carol, Parada Luis F, Ramirez Francesco, ;2005;Molecular and cellular biology;25;5699-711; 15964824
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