About   Help   FAQ
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





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/19/2024
MGI 6.24
The Jackson Laboratory