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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gdpd5tm1.1Itl
targeted mutation 1.1, inGenious Targeting Laboratory
MGI:5302017
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Gdpd5tm1.1Itl/Gdpd5tm1.1Itl involves: 129 * C57BL/6J MGI:5302060
cn2
Gdpd5tm1Itl/Gdpd5tm1.1Itl
Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
involves: 129S1/Sv * 129/Sv * 129X1/SvJ * C57BL/6J MGI:5302059
cx3
Gdpd5tm1.1Itl/Gdpd5tm1.1Itl
Tg(Hlxb9-GFP)1Tmj/0
involves: 129/Sv * C57BL/6 * C57BL/6J * CBA MGI:5302061


Genotype
MGI:5302060
hm1
Allelic
Composition
Gdpd5tm1.1Itl/Gdpd5tm1.1Itl
Genetic
Background
involves: 129 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gdpd5tm1.1Itl mutation (0 available); any Gdpd5 mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• mice exhibit reduced formation of motor neurons compared with wild-type mice
• at P5 and P28, alpha motor neuron differentiation is impaired in the lateral motor neurons
• however, no increase in apoptosis is observed and lateral motor column gamma motor neurons and medial motor column alpha and gamma motor neurons are intact
• fewer motor neuron progenitors exit the cell cycle and exhibit extended cell cycle compared to in wild-type mice
• at E11.5 and E13.5 in lateral motor neurons
• at E12.5, but not E13.5, in the lateral motor neurons of the adductor longus and magnus and posterior gracilis muscles
• at E13.5 in hypaxial motor neurons
• at E13.5 in the rectofemoratibialis muscles
• at E13.5 and E14.5 in the medial anterior gracilis, medial adductor brevis, and vasti muscles
• however, the number of medial motor neurons or preganglionic columns are normal

cellular
• mice exhibit reduced formation of motor neurons compared with wild-type mice
• at P5 and P28, alpha motor neuron differentiation is impaired in the lateral motor neurons
• however, no increase in apoptosis is observed and lateral motor column gamma motor neurons and medial motor column alpha and gamma motor neurons are intact
• fewer motor neuron progenitors exit the cell cycle and exhibit extended cell cycle compared to in wild-type mice




Genotype
MGI:5302059
cn2
Allelic
Composition
Gdpd5tm1Itl/Gdpd5tm1.1Itl
Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
Genetic
Background
involves: 129S1/Sv * 129/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gdpd5tm1.1Itl mutation (0 available); any Gdpd5 mutation (37 available)
Gdpd5tm1Itl mutation (0 available); any Gdpd5 mutation (37 available)
Gt(ROSA)26Sortm1(cre/ERT)Nat mutation (2 available); any Gt(ROSA)26Sor mutation (993 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• mice treated with tamoxifen after neurogenesis (at E10.5) exhibit normal motor pool formation
• mice treated with tamoxifen at E8.5 exhibit delayed motor neuron formation compared with control mice
• at E12.5, mice treated with tamoxifen at E8.5 exhibit fewer Isl1/2+ and vasti, adductor longus and magnus, and posterior gracilis muscle motor neurons compared with control mice
• at E14.5, mice treated with tamoxifen at E8.5 exhibit fewer Isl1/2+ and vasti muscle motor neurons compared with control mice
• however, motor neurons in adductor longus and magnus and posterior gracilis muscles recover by E14.5

cellular
• mice treated with tamoxifen at E8.5 exhibit delayed motor neuron formation compared with control mice




Genotype
MGI:5302061
cx3
Allelic
Composition
Gdpd5tm1.1Itl/Gdpd5tm1.1Itl
Tg(Hlxb9-GFP)1Tmj/0
Genetic
Background
involves: 129/Sv * C57BL/6 * C57BL/6J * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gdpd5tm1.1Itl mutation (0 available); any Gdpd5 mutation (37 available)
Tg(Hlxb9-GFP)1Tmj mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• mice exhibit thinner major axonal tracts emerging from lumbosacral segment 2 compared with wild-type mice
• however, existing lateral motor neurons at E12.5 and E14.5 are normal
• mice exhibit a delay and loss of lumbosacral segment motor neuron pools compared with wild-type mice





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory