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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Dclk1tm1Caw
targeted mutation 1, Christopher A Walsh
MGI:3626361
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Dclk1tm1Caw/Dclk1tm1Caw involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J MGI:3628588
cx2
Dclk1tm1Caw/Dclk1tm1Caw
Dcxtm1Caw/Y
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J MGI:3628582
cx3
Dclk1tm1Caw/Dclk1tm1Caw
Dcxtm1Caw/Dcx+
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J MGI:3628584
cx4
Dclk1tm1Caw/Dclk1+
Dcxtm1Caw/Dcx+
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J MGI:3628593
cx5
Dclk1tm1Caw/Dclk1+
Dcxtm1Caw/Y
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J MGI:3628602


Genotype
MGI:3628588
hm1
Allelic
Composition
Dclk1tm1Caw/Dclk1tm1Caw
Genetic
Background
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dclk1tm1Caw mutation (0 available); any Dclk1 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• cortical neurons from Dcamkl1-null embryos transfected with Dcx RNAi show aberrant processes; dendritic processes appear shorter and more numerous than control Dcamkl1-deficient neurons and many cells appear to lack a primary dendrite
• cortical neurons from Dcamkl1-null embryos transfected with Dcx RNAi have much shorter axons than wild-type neurons transfected with Dcx RNAi (230 microns vs 702 microns)




Genotype
MGI:3628582
cx2
Allelic
Composition
Dclk1tm1Caw/Dclk1tm1Caw
Dcxtm1Caw/Y
Genetic
Background
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dclk1tm1Caw mutation (0 available); any Dclk1 mutation (53 available)
Dcxtm1Caw mutation (0 available); any Dcx mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• more than 75% of double knockouts die within 2 days of birth

nervous system
• double knockouts exhibit disruption of most or all major axon tracts in the brain; brains of double knockouts display severely disorganized white-matter tracts
• cerebellum of mutants has defective foliation; folia are severely hypoplastic, particularly on the ventral surface of the cerebellum
• there are no fibers crossing the midline of the corpus callosum; most axons end before reaching the midline and do not cross to the other side
• axons appear as multiple single axons with random orientation and without clear fasciculation rather than bundles
• in mutants, corpus callosum is present at rostral levels but does not extend as far caudally as in wild-type mice; anterior portion is greatly reduced in thickness
• hippocampal commissures appear lumpy and disorganized
• aberrant anterior commissure bundles are observed
• in some animals, internal capsule has abnormal morphology
• there is absence of an internal capsule in the striatum
• disruption of many brainstem nuclei is observed
• there is absence of pencil fibers in the striatum
• disruption of many thalamic nuclei is observed
• stratum pyramidale layer in pyramidal cell fields, CA3,CA2and CA1 is disorganized with multiple cell layers separated by irregular streams of white matter
• at P0, there is disruption of lamination of the cerebral cortex in the cingulate gyrus in double knockouts
• brains of double knockouts at P0 display a thin cerebral cortex
• no axons leave the region of the entorhinal cortex
• subcortical white matter appears lumpy and disorganized
• cells appear less tightly packed
• there is markedly abnormal cell layering in the hippocampus
• the cerebellum is small in double knockouts




Genotype
MGI:3628584
cx3
Allelic
Composition
Dclk1tm1Caw/Dclk1tm1Caw
Dcxtm1Caw/Dcx+
Genetic
Background
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dclk1tm1Caw mutation (0 available); any Dclk1 mutation (53 available)
Dcxtm1Caw mutation (0 available); any Dcx mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• fertility appears to be reduced




Genotype
MGI:3628593
cx4
Allelic
Composition
Dclk1tm1Caw/Dclk1+
Dcxtm1Caw/Dcx+
Genetic
Background
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dclk1tm1Caw mutation (0 available); any Dclk1 mutation (53 available)
Dcxtm1Caw mutation (0 available); any Dcx mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• fertility appears to be reduced




Genotype
MGI:3628602
cx5
Allelic
Composition
Dclk1tm1Caw/Dclk1+
Dcxtm1Caw/Y
Genetic
Background
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dclk1tm1Caw mutation (0 available); any Dclk1 mutation (53 available)
Dcxtm1Caw mutation (0 available); any Dcx mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• a slightly lower proportion of Dcx-deficient, Dcamkl1-heterozygous males die postnatally than double knockouts

nervous system
• mutants have less severe and less penetrant white matter defects than double knockouts
• lateral ventricles are enlarged in mutants
• some animals have an absent corpus callosum





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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory