About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mst1tm1Jab
targeted mutation 1, Jorge A Bezerra
MGI:2445230
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Mst1tm1Jab/Mst1tm1Jab involves: 129P2/OlaHsd * Black Swiss MGI:3531095


Genotype
MGI:3531095
hm1
Allelic
Composition
Mst1tm1Jab/Mst1tm1Jab
Genetic
Background
involves: 129P2/OlaHsd * Black Swiss
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mst1tm1Jab mutation (0 available); any Mst1 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Livers of Mst1tm1Jab/Mst1tm1Jab mice display cytoplasmic vacuolization of hepatocytes

digestive/alimentary system
N
• homozygotes display normal weight gain and stooling pattern with no evidence of histopathologic abnormality along the digestive tract
• in response to acute chemically-induced colitis, mutants appear to be more affected by 5% dextran sulfate sodium (DSS) than wild-type mice (based on diarrhea, visible blood in stools, weight loss)
• however, 7 days after DSS, homozygotes show no significant differences in these parameters or in colonic histology relative to wild-type mice

growth/size/body
N
• homozygotes are viable, fertile, overtly normal, and display no differences in weight gain relative to wild-type

hematopoietic system
N
• bone marrow aspirates indicate similar myelocytic, erythrocytic, and megakaryocytic lineages in mutant and wild-type mice
• mutants display no differences in the number or morphology of circulating erythrocytes, leukocytes or platelets relative to wild-type
• in vitro, homozygotes show delayed activation of resident peritoneal macrophages in the first 13 h of incubation with serum; however, activation is gradually increased reaching wild-type levels by 21-24 h
• in vivo, homozygotes show normal migration of mononuclear phagocytes into the peritoneal cavity and normal activation of peritoneal macrophages 72 h after thioglycollate injection

immune system
N
• homozygotes display normal healing of excisional skin wounds relative to wild-type
• in response to acute chemically-induced colitis, mutants appear to be more affected by 5% dextran sulfate sodium (DSS) than wild-type mice (based on diarrhea, visible blood in stools, weight loss)
• however, 7 days after DSS, homozygotes show no significant differences in these parameters or in colonic histology relative to wild-type mice
• in vitro, homozygotes show delayed activation of resident peritoneal macrophages in the first 13 h of incubation with serum; however, activation is gradually increased reaching wild-type levels by 21-24 h
• in vivo, homozygotes show normal migration of mononuclear phagocytes into the peritoneal cavity and normal activation of peritoneal macrophages 72 h after thioglycollate injection

liver/biliary system
N
• mutant livers appear macroscopically normal
• in addition, serum biochemical indicators of hepatic synthetic and excretory functions appear unaffected relative to wild-type
• at 1-6 mo of age, mutant livers display varying degrees of cytoplasmic vacuolization of hepatocytes; all other organs appear normal
• no hepatic inflammation or changes in the bile duct or other nonparenchymal cells are obseved
• cytoplasmic vacuolizations are found in 79% of homozygotes, contain lipid, and are distributed uniformly throughout the liver lobule
• such vacuolizations are detected at 1 month of age and do not appear to progress up to 6 months; however, in some livers the lesion is severe





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
12/10/2024
MGI 6.24
The Jackson Laboratory