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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Dcctm1Wbg
targeted mutation 1, Robert A Weinberg
MGI:1934924
Summary 8 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Dcctm1Wbg/Dcctm1Wbg B6.129S2-Dcctm1Wbg MGI:3665466
hm2
Dcctm1Wbg/Dcctm1Wbg involves: 129S2/SvPas MGI:2446653
hm3
Dcctm1Wbg/Dcctm1Wbg Not Specified MGI:2446656
ht4
Dcctm1Wbg/Dcc+ involves: 129S2/SvPas * C57BL/6 MGI:2446652
ht5
Dcckanga/Dcctm1Wbg involves: 129X1/SvJ * AKR * C3H MGI:3665462
cx6
Dcctm1Wbg/Dcc+
Unc5crcmTg(Ucp)1.23Kz/Unc5c+
involves: 129X1/SvJ * C57BL/6J * SJL/J MGI:3665461
cx7
Dcctm1Wbg/Dcc+
Unc5crcmTg(Ucp)1.23Kz/Unc5crcmTg(Ucp)1.23Kz
involves: 129X1/SvJ * C57BL/6J * SJL/J MGI:3665460
cx8
ApcMin/Apc+
Dcctm1Wbg/Dcc+
involves: C57BL/6J MGI:2446655


Genotype
MGI:3665466
hm1
Allelic
Composition
Dcctm1Wbg/Dcctm1Wbg
Genetic
Background
B6.129S2-Dcctm1Wbg
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dcctm1Wbg mutation (1 available); any Dcc mutation (76 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• no trochlear nerve abnormalities are detected at E11.5 and diaphragm innervation is similar to wild-type at E18.5
• at E13.5 ectopic motor neurons are found to have migrated out of the ventral horn and into the root, with 42% of roots having ectopic neurons and an average of 1.7 cells per root




Genotype
MGI:2446653
hm2
Allelic
Composition
Dcctm1Wbg/Dcctm1Wbg
Genetic
Background
involves: 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dcctm1Wbg mutation (1 available); any Dcc mutation (76 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice died within 24 hours of birth

behavior/neurological
• mice appeared unable to suckle

respiratory system
• mice exhibited labored respirations

nervous system
• some misrouting of commissural axons that projected into the ventral spinal cord
• absent hippocampal commissure
• absence of pontine nuclei from the hindbrain
• reduction in the number of commissural axons with the dorsal spinal cord of mice examined at E9.5-E11.5

cellular
• some misrouting of commissural axons that projected into the ventral spinal cord




Genotype
MGI:2446656
hm3
Allelic
Composition
Dcctm1Wbg/Dcctm1Wbg
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dcctm1Wbg mutation (1 available); any Dcc mutation (76 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• hypopigmented streaks in E15-E16 embryos

vision/eye
• small optic discs in E15-E16 embryos; optic nerve hypoplasia
• retinal ganglion cells failed to exit the optic nerve and were misrouted to other regions of the eye
• hypopigmented streaks in E15-E16 embryos

nervous system
• small optic discs in E15-E16 embryos; optic nerve hypoplasia
• retinal ganglion cells failed to exit the optic nerve and were misrouted to other regions of the eye




Genotype
MGI:2446652
ht4
Allelic
Composition
Dcctm1Wbg/Dcc+
Genetic
Background
involves: 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dcctm1Wbg mutation (1 available); any Dcc mutation (76 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
N
• no significant increase in tumor predisposition was noted in heterozygous mice when compared to controls




Genotype
MGI:3665462
ht5
Allelic
Composition
Dcckanga/Dcctm1Wbg
Genetic
Background
involves: 129X1/SvJ * AKR * C3H
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dcckanga mutation (1 available); any Dcc mutation (76 available)
Dcctm1Wbg mutation (1 available); any Dcc mutation (76 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological

nervous system
• axons fail to cross the midline at the pyramidal decussation and instead extend into the lateral and ventral funiculus
• absent hippocampal commissure
• no axons cross the midline at the pyramidal decussation
• absent from the dorsal funiculus

cellular
• axons fail to cross the midline at the pyramidal decussation and instead extend into the lateral and ventral funiculus




Genotype
MGI:3665461
cx6
Allelic
Composition
Dcctm1Wbg/Dcc+
Unc5crcmTg(Ucp)1.23Kz/Unc5c+
Genetic
Background
involves: 129X1/SvJ * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dcctm1Wbg mutation (1 available); any Dcc mutation (76 available)
Unc5crcmTg(Ucp)1.23Kz mutation (0 available); any Unc5c mutation (61 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• a few axons fail to cross the midline at the pyramidal decussation and instead extend into the ventral funiculus of the cervical spinal cord

cellular
• a few axons fail to cross the midline at the pyramidal decussation and instead extend into the ventral funiculus of the cervical spinal cord




Genotype
MGI:3665460
cx7
Allelic
Composition
Dcctm1Wbg/Dcc+
Unc5crcmTg(Ucp)1.23Kz/Unc5crcmTg(Ucp)1.23Kz
Genetic
Background
involves: 129X1/SvJ * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dcctm1Wbg mutation (1 available); any Dcc mutation (76 available)
Unc5crcmTg(Ucp)1.23Kz mutation (0 available); any Unc5c mutation (61 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• some axons fail to cross the midline at the pyramidal decussation and instead extend into the lateral and ventral funiculus

cellular
• some axons fail to cross the midline at the pyramidal decussation and instead extend into the lateral and ventral funiculus




Genotype
MGI:2446655
cx8
Allelic
Composition
ApcMin/Apc+
Dcctm1Wbg/Dcc+
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
ApcMin mutation (12 available); any Apc mutation (154 available)
Dcctm1Wbg mutation (1 available); any Dcc mutation (76 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• heterozygosity for the Dcc allele did not affect the polyp initiation or average size or morphology of the adenomas that occur in the ApcMin heterozygous mice

digestive/alimentary system
• heterozygosity for the Dcc allele did not affect the polyp initiation or average size or morphology of the adenomas that occur in the ApcMin heterozygous mice





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory