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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Lasp1Tg(Col1a1-lacZ)1Ngma
transgene insertion 1, N Gmachl
MGI:2441658
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Lasp1Tg(Col1a1-lacZ)1Ngma/Lasp1Tg(Col1a1-lacZ)1Ngma involves: C57BL/6 MGI:4366487
hm2
Lasp1Tg(Col1a1-lacZ)1Ngma/Lasp1Tg(Col1a1-lacZ)1Ngma Not Specified MGI:2445231
cx3
Lasp1Tg(Col1a1-lacZ)1Ngma/Lasp1Tg(Col1a1-lacZ)1Ngma
Pax1un-ex/Pax1un-ex
involves: C57BL/6 MGI:4366488


Genotype
MGI:4366487
hm1
Allelic
Composition
Lasp1Tg(Col1a1-lacZ)1Ngma/Lasp1Tg(Col1a1-lacZ)1Ngma
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lasp1Tg(Col1a1-lacZ)1Ngma mutation (0 available); any Lasp1 mutation (170 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all mice treated with a low dose of retinoic acid at E9 die perinatally unlike similarly treated wild-type mice

skeleton
• at P10, neural arches in the lumbar region remain open in 50% of mice unlike in wild-type mice
• however, the neural arches close by P14
• sternum ossification centers in retinoic acid treated mice are shifted resulting in a crankshaft sternum unlike in similarly treated wild-type mice
• deformed and wedge-shaped in the tail with fewer proliferating cells
• 8 of 11 retinoic acid-treated mice lack the sixth vertebra unlike similarly treated wild-type mice
• at P10, the vertebral growth plate in the tail is compressed and disrupted die to thinner zones of proliferating and hypertrophic cartilage compared to in wild-type mice
• fewer proliferating cells are present in the growth plate of tail vertebrae compared to in wild-type mice
• at P10, neural arches lack processus spinosi unlike in wild-type mice
• in the tail
• 50% of retinoic acid treated mice exhibit a loss of ossification centers in cervical vertebrae unlike in similarly treated wild-type mice

homeostasis/metabolism
• all mice treated with a low dose of retinoic acid at E9 die perinatally unlike similarly treated wild-type mice
• 50% of retinoic acid treated mice exhibit a loss of ossification centers in cervical vertebrae unlike in similarly treated wild-type mice
• 8 of 11 retinoic acid-treated mice lack the sixth vertebra unlike similarly treated wild-type mice
• sternum ossification centers in retinoic acid treated mice are shifted resulting in a crankshaft sternum unlike in similarly treated wild-type mice
• retinoic acid treated mice have cleft palates resulting in breathing difficulties and premature death unlike similarly treated wild-type mice
• treatment with folic acid does not improve incidence of spina bifida occulta

limbs/digits/tail
• at P15, mice have several bends, but not kinks, in its tail unlike wild-type mice

craniofacial
• in retinoic acid treated mice unlike similarly treated wild-type mice

nervous system
• at P10, neural arches in the lumbar region remain open in 50% of mice unlike in wild-type mice
• however, the neural arches close by P14

embryo
• at P10, neural arches in the lumbar region remain open in 50% of mice unlike in wild-type mice
• however, the neural arches close by P14

digestive/alimentary system
• in retinoic acid treated mice unlike similarly treated wild-type mice

growth/size/body
• in retinoic acid treated mice unlike similarly treated wild-type mice




Genotype
MGI:2445231
hm2
Allelic
Composition
Lasp1Tg(Col1a1-lacZ)1Ngma/Lasp1Tg(Col1a1-lacZ)1Ngma
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lasp1Tg(Col1a1-lacZ)1Ngma mutation (0 available); any Lasp1 mutation (170 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• severe scoliosis of the tail vertebral column
• delayed closure of the vertebral arches in the lumbar region




Genotype
MGI:4366488
cx3
Allelic
Composition
Lasp1Tg(Col1a1-lacZ)1Ngma/Lasp1Tg(Col1a1-lacZ)1Ngma
Pax1un-ex/Pax1un-ex
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lasp1Tg(Col1a1-lacZ)1Ngma mutation (0 available); any Lasp1 mutation (170 available)
Pax1un-ex mutation (1 available); any Pax1 mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• rib joints are thickened compared to in wild-type mice
• lumbar vertebra are compressed with split vertebrae that fail to fuse unlike in wild-type mice
• the lumbar vertebra are compressed

limbs/digits/tail
• during the first weak after birth, mice exhibit a sharp hair pin-like upturn in their tails immediately after the last sacral vertebrae that is more severe than in single homozygotes
• mice develop kicks and strong bends in their tails





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