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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rock1tm1Liao
targeted mutation 1, James K Liao
MGI:3665285
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Rock1tm1Liao/Rock1+ C57BL/6-Rock1tm1Liao MGI:3687016


Genotype
MGI:3687016
ht1
Allelic
Composition
Rock1tm1Liao/Rock1+
Genetic
Background
C57BL/6-Rock1tm1Liao
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rock1tm1Liao mutation (0 available); any Rock1 mutation (60 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• following carotid artery ligation, vascular smooth muscle proliferation and survival are decreased compared to in wild-type mice
• thrombin-stimulated endothelial cells do not exhibit U937-LAM (U937 monocytes expressing human L selectin) adherence under laminar flow unlike wild-type cells
• flow cessation caused by ligation of the left common carotid artery produces a smaller increase in neointima formation than in wild-type mice due to decreased proliferation
• bone marrow derived cells form decreased neointima after carotid ligation compared to wild-type bone marrow-derived cells
• however, mice transplanted with wild-type bone marrow exhibit normal neointima formation following carotid artery ligation

immune system
• following carotid artery ligation, recruitment of leukocyte is decreased compared to in wild-type mice
• following thioglycollate-induced peritonitis, leukocyte chemotaxis, accumulation and adherence are impaired compared to in wild-type mice
• mice receiving bone marrow transplants exhibit decreased leukocyte recruitment following carotid artery ligation compared to mice receiving wild-type bone marrow transfers
• following carotid artery ligation or thioglycollate-induced peritonitis, recruitment of macrophage is decreased compared to in wild-type mice
• impaired following thioglycollate-induced peritonitis
• following thioglycollate-induced peritonitis

muscle
• following carotid artery ligation, vascular smooth muscle proliferation and survival are decreased compared to in wild-type mice

homeostasis/metabolism
• flow cessation caused by ligation of the left common carotid artery produces a smaller increase in neointima formation than in wild-type mice due to decreased proliferation
• bone marrow derived cells form decreased neointima after carotid ligation compared to wild-type bone marrow-derived cells
• however, mice transplanted with wild-type bone marrow exhibit normal neointima formation following carotid artery ligation

respiratory system
• exposure of murine lung endothelial cells to high glucose conditions fails to increase Serpine1 protein levels as in wild-type murine lung endothelial cells

cellular
• following carotid artery ligation, recruitment of leukocyte is decreased compared to in wild-type mice
• following thioglycollate-induced peritonitis, leukocyte chemotaxis, accumulation and adherence are impaired compared to in wild-type mice
• mice receiving bone marrow transplants exhibit decreased leukocyte recruitment following carotid artery ligation compared to mice receiving wild-type bone marrow transfers
• following carotid artery ligation or thioglycollate-induced peritonitis, recruitment of macrophage is decreased compared to in wild-type mice
• impaired following thioglycollate-induced peritonitis

hematopoietic system
• following carotid artery ligation, recruitment of leukocyte is decreased compared to in wild-type mice
• following thioglycollate-induced peritonitis, leukocyte chemotaxis, accumulation and adherence are impaired compared to in wild-type mice
• mice receiving bone marrow transplants exhibit decreased leukocyte recruitment following carotid artery ligation compared to mice receiving wild-type bone marrow transfers
• following carotid artery ligation or thioglycollate-induced peritonitis, recruitment of macrophage is decreased compared to in wild-type mice
• impaired following thioglycollate-induced peritonitis
• following thioglycollate-induced peritonitis





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