About   Help   FAQ
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 (169 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 (169 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 (169 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





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
05/07/2024
MGI 6.23
The Jackson Laboratory