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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Kidins220tm1.2Fces
targeted mutation 1.2, Fabrizia Cesca
MGI:5527339
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Kidins220tm1.2Fces/Kidins220tm1.2Fces involves: 129 * BALB/c * C57BL/6 * C57BL/6J MGI:5527357


Genotype
MGI:5527357
hm1
Allelic
Composition
Kidins220tm1.2Fces/Kidins220tm1.2Fces
Genetic
Background
involves: 129 * BALB/c * C57BL/6 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kidins220tm1.2Fces mutation (1 available); any Kidins220 mutation (79 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• despite being present in Mendelian ratios at E15, mice die before birth

nervous system
N
• neuron proliferation in the central nervous system is normal
• poorly vascularized brains corresponding to regions of increased apoptosis
• abnormal vascular patterning and larger vessel diameter at E16.5 and E18.5
• glomeruloid terminal structures form in the subventricular zone
• at E13.5 in the dorsal root ganglion at the thoracic and lumbar levels affecting all neuronal subtypes
• at E14.5 in vestibular and glossopharyngeal ganglia
• at E15.5 and E16.5 in the ventral neuroepithelium, retina, thalamus and cortex
• at E18.5 in the neuroepithelium, subventricular zone, cingulum and dorsal subiculum of the hippocampus, cortex, caudate putamen, ventroposterolateral and medial thalamic nuclei and nucleus reuniens
• more severe during development
• hippocampal nerves exhibit altered response to BDNF with increased axonal length, number of dendrites, decreased branching dendrites and decreased dendrite length compared with wild-type cells
• however, axonal growth in response to BDNF is normal
• in the lumbar spinal cord at E18.5
• increased number of axon branches and axonal length in untreated neurons
• however, axonal growth in response to BDNF is normal
• hippocampal nerves exhibit altered response to BDNF with increased axonal length, number of dendrites, decreased branching dendrites and decreased dendrite length compared with wild-type cells
• impaired BDNF-induced excitatory postsynaptic current potentiation
• however, mice exhibit normal excitatory postsynaptic current amplitude and paired-pulse potentiation

cardiovascular system
• poorly vascularized brains corresponding to regions of increased apoptosis
• abnormal vascular patterning and larger vessel diameter at E16.5 and E18.5
• glomeruloid terminal structures form in the subventricular zone
• dilated and congested atria at E18.5
• vacuolated and disorganized wall
• in the brain

growth/size/body

vision/eye
• increased at E15.5 and E16.5

cellular
• at E13.5 in the dorsal root ganglion at the thoracic and lumbar levels affecting all neuronal subtypes
• at E14.5 in vestibular and glossopharyngeal ganglia
• at E15.5 and E16.5 in the ventral neuroepithelium, retina, thalamus and cortex
• at E18.5 in the neuroepithelium, subventricular zone, cingulum and dorsal subiculum of the hippocampus, cortex, caudate putamen, ventroposterolateral and medial thalamic nuclei and nucleus reuniens
• more severe during development
• increased at E15.5 and E16.5
• hippocampal nerves exhibit altered response to BDNF with increased axonal length, number of dendrites, decreased branching dendrites and decreased dendrite length compared with wild-type cells
• however, axonal growth in response to BDNF is normal





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory