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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Katna1tm1a(KOMP)Wtsi
targeted mutation 1a, Wellcome Trust Sanger Institute
MGI:4458514
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Katna1tm1a(KOMP)Wtsi/Katna1tm1a(KOMP)Wtsi involves: C57BL/6J * C57BL/6N MGI:6401101
ht2
Katna1tm1a(KOMP)Wtsi/Katna1+ involves: C57BL/6J * C57BL/6N MGI:6401102


Genotype
MGI:6401101
hm1
Allelic
Composition
Katna1tm1a(KOMP)Wtsi/Katna1tm1a(KOMP)Wtsi
Genetic
Background
involves: C57BL/6J * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Katna1tm1a(KOMP)Wtsi mutation (2 available); any Katna1 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no viable homozygous mice were obtained out of 149 mice born; one necrotic homozygous embryo was obtained at E15 but not at later stages




Genotype
MGI:6401102
ht2
Allelic
Composition
Katna1tm1a(KOMP)Wtsi/Katna1+
Genetic
Background
involves: C57BL/6J * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Katna1tm1a(KOMP)Wtsi mutation (2 available); any Katna1 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mice show no deficits in hippocampal-dependent spatial and contextual learning and memory tasks relative to wild-type controls

cellular
• mice show delayed neuronal proliferation in the cortical neurogenic niche, with significant accumulation of neuronal progenitors at the ventricular/subventricular zone during corticogenesis
• however, no malformation or aberrant cell distribution of cortical layers II, III, IV V or VI is observed during embryonic development or at early postnatal stages
• adult mice show a ~50% reduction in the number of proliferating BrdU-positive cells in the subgranular zone (SGZ) of the dentate gyrus

nervous system
N
• adult brain size and overall brain anatomy are normal; no evidence of apoptosis or neuronal degeneration is observed
• adult mice show no deficits in long-term potentiation (LTP) at the dentate gyrus relative to wild-type controls
• Sholl analysis of dentate gyrus granule cells revealed normal dendritic arborization
• mice show delayed neuronal proliferation in the cortical neurogenic niche, with significant accumulation of neuronal progenitors at the ventricular/subventricular zone during corticogenesis
• however, no malformation or aberrant cell distribution of cortical layers II, III, IV V or VI is observed during embryonic development or at early postnatal stages
• adult mice show a ~50% reduction in the number of proliferating BrdU-positive cells in the subgranular zone (SGZ) of the dentate gyrus
• mice exhibit an accumulation of immature doublecortin (DCX)-positive cells (neuronal precursors and newborn post-mitotic neurons) in the subgranular zone (SGZ) of the dentate gyrus during adult hippocampal neurogenesis
• Sox2/GFAP double-immunostaining revealed a significant increase in immature type-1 neuronal precursor cells in the subgranular zone (SGZ) of the adult dentate gyrus





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory