normal phenotype
• heterozygotes are viable, fertile and do not exhibit any apparent phenotype, size change or other abnormality relative to wild-type controls
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Allele Symbol Allele Name Allele ID |
Trim71+ wild type MGI:3611275 |
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Summary |
3 genotypes
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• heterozygotes are viable, fertile and do not exhibit any apparent phenotype, size change or other abnormality relative to wild-type controls
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Data Sources
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
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IMPC - UCD
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IMPC - UCD
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♀ | phenotype observed in females |
♂ | phenotype observed in males |
N | normal phenotype |
• E9.5 neuroepithelia of embryos has fewer pH3+ cells (cell proliferation marker) and more DCX+ cells (marker of immature neurons)
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• fetal hydrocephalus
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• P0 hydrocephalic mice exhibit patency of the midbrain cerebral aqueduct (aqueductal stenosis) but the aqueduct narrows by P21
• however, ependymal and choroid plexus cells appear morphologically normal in P0 hydrocephalic mice
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• severe ventriculomegaly is detectable at birth (P0) in approximately 16% mice
• by P21, hydrocephalic mice exhibit progressive ventriculomegaly associated with macrocephaly and doming of the skull
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• mice at birth show ventriculomegaly with decreased cerebral cortex volume (cerebrocortical hypoplasia) despite normal intracranial volume
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• hydrocephalic mice exhibit a thinned cerebral cortex at P0 with reduced thickness of the superficial and deep cortical layers
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• cortical neurogenesis: marker analysis shows reduced numbers of neurons in cortical layers in hydrocephalic mice at P0
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• intracranial pressure is elevated at P7 in hydrocephalic mice
• mice show abnormal brain-fluid biomechanics, showing a reduction in stiffness and relaxation modulus and increased compliance in P7 hydrocephalic brain tissues, suggesting that brains are hypercompliant and less able to resist mechanical strain, leading to accommodation of greater CSF volume at any given CSF pressure
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• subventricular zone neural proliferation is reduced in hydrocephalic mice at P0
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• hydrocephalic mice show impaired cerebrospinal fluid (CSF) outflow from the forebrain ventricles
• however, ependymal cilia-generated CSF flow is unaffected in P7 hydrocephalic mice
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• E9.5 neuroepithelia of embryos has fewer pH3+ cells, indicating decreased cell proliferation
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• embryonic stem cells are less proliferative than wild-type stem cells upon N2B27-induced neural differentiation
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• hydrocephalic mice eventually exhibit progressive macrocephaly by P21
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• intracranial volume is increased in P21 hydrocephalic mice but not at P0
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• doming of the skull is seen by P21
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• subventricular zone neural proliferation is reduced in hydrocephalic mice at P0
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• intracranial volume is increased in P21 hydrocephalic mice but not at P0
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• doming of the skull is seen by P21
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• E9.5 neuroepithelia of embryos has fewer pH3+ cells (cell proliferation marker) and more DCX+ cells (marker of immature neurons)
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Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
hydrocephalus | DOID:10908 |
OMIM:123155 OMIM:236600 OMIM:236635 OMIM:307000 OMIM:615219 |
J:335575 |
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 03/18/2025 MGI 6.24 |
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