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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Dclk1+
wild type
MGI:2437351
Summary 8 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
\Dclk1tm1a(EUCOMM)Wtsi/\Dclk1+ C57BL/6N-Dclk1tm1a(EUCOMM)Wtsi/Wtsi MGI:5797468
ht2
\Dclk1tm1.1Jgg/\Dclk1+ involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 MGI:3618287
cn3
\ApcMin/\Apc+
\Dclk1tm1.1(cre/ERT2)Seno/\Dclk1+
\Gt(ROSA)26Sortm1Sor/\Gt(ROSA)26Sortm1(HBEGF)Awai
involves: 129S4/SvJaeSor * C57BL/6 MGI:5475206
cn4
\Ctnnb1tm1Mmt/\Ctnnb1+
\Dclk1tm1.1(cre/ERT2)Seno/\Dclk1+
involves: 129X1/SvJ * C57BL/6 MGI:5475208
cx5
\Dclk1tm1.1Jgg/\Dclk1+
\Dcxtm1Caw/\Dcxtm1Caw
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 MGI:3618311
cx6
\Dclk1tm1.1Jgg/\Dclk1+
\Dcxtm1Caw/Y
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 MGI:3618308
cx7
\Dclk1tm1Caw/\Dclk1+
\Dcxtm1Caw/\Dcx+
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J MGI:3628593
cx8
\Dclk1tm1Caw/\Dclk1+
\Dcxtm1Caw/Y
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J MGI:3628602


Genotype
MGI:5797468
ht1
Allelic
Composition
\Dclk1tm1a(EUCOMM)Wtsi/\Dclk1+
Genetic
Background
C57BL/6N-Dclk1tm1a(EUCOMM)Wtsi/Wtsi
Cell Lines MEPD1000_3_H02
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dclk1tm1a(EUCOMM)Wtsi mutation (1 available); any Dclk1 mutation (56 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological

immune system




Genotype
MGI:3618287
ht2
Allelic
Composition
\Dclk1tm1.1Jgg/\Dclk1+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dclk1tm1.1Jgg mutation (0 available); any Dclk1 mutation (56 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• alterations in corpus callosum thickness are observed in heterozygotes with the appearance of small Probst bundles




Genotype
MGI:5475206
cn3
Allelic
Composition
\ApcMin/\Apc+
\Dclk1tm1.1(cre/ERT2)Seno/\Dclk1+
\Gt(ROSA)26Sortm1Sor/\Gt(ROSA)26Sortm1(HBEGF)Awai
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
ApcMin mutation (12 available); any Apc mutation (156 available)
Dclk1tm1.1(cre/ERT2)Seno mutation (0 available); any Dclk1 mutation (56 available)
Gt(ROSA)26Sortm1(HBEGF)Awai mutation (4 available); any Gt(ROSA)26Sor mutation (1097 available)
Gt(ROSA)26Sortm1Sor mutation (10 available); any Gt(ROSA)26Sor mutation (1097 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• after tamoxifen treatment and a single injection of diphtheria toxin (DT), polyps contain many Dclk1-positive apoptotic tumor cells and are severely injured or collapsed with Dclk1-negative polyps not displaying DT-induced apoptosis

digestive/alimentary system
N
• after tamoxifen treatment and multiple diphtheria toxin injections to ablate Dclk1-positive cells, these cells are absent from the normal intestine with no significant damage to organ architecture observed in the intestine or stomach

endocrine/exocrine glands
N
• after tamoxifen treatment and multiple diphtheria toxin injections to ablate Dclk1-positive cells, no significant damage in organ architecture is observed in the pancreas or gallbladder




Genotype
MGI:5475208
cn4
Allelic
Composition
\Ctnnb1tm1Mmt/\Ctnnb1+
\Dclk1tm1.1(cre/ERT2)Seno/\Dclk1+
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctnnb1tm1Mmt mutation (0 available); any Ctnnb1 mutation (47 available)
Dclk1tm1.1(cre/ERT2)Seno mutation (0 available); any Dclk1 mutation (56 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
N
• 40 days after tamoxifen treatment, mice show no detectable polyp development in the small intestine




Genotype
MGI:3618311
cx5
Allelic
Composition
\Dclk1tm1.1Jgg/\Dclk1+
\Dcxtm1Caw/\Dcxtm1Caw
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dclk1tm1.1Jgg mutation (0 available); any Dclk1 mutation (56 available)
Dcxtm1Caw mutation (0 available); any Dcx mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• corpus callosum is absent




Genotype
MGI:3618308
cx6
Allelic
Composition
\Dclk1tm1.1Jgg/\Dclk1+
\Dcxtm1Caw/Y
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dclk1tm1.1Jgg mutation (0 available); any Dclk1 mutation (56 available)
Dcxtm1Caw mutation (0 available); any Dcx mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• corpus callosum is hypoplastic
• anterior commissure is severely reduced in thickness
• cortical neuron distribution is altered, with neurons showing a much broader pattern of distribution




Genotype
MGI:3628593
cx7
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 (56 available)
Dcxtm1Caw mutation (0 available); any Dcx mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• fertility appears to be reduced




Genotype
MGI:3628602
cx8
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 (56 available)
Dcxtm1Caw mutation (0 available); any Dcx mutation (19 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
03/25/2025
MGI 6.24
The Jackson Laboratory