About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fem1atm1Seno
targeted mutation 1, Hiroshi Seno
MGI:6150325
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Fem1atm1Seno/Fem1atm1Seno C57BL/6-Fem1atm1Seno MGI:6151409


Genotype
MGI:6151409
hm1
Allelic
Composition
Fem1atm1Seno/Fem1atm1Seno
Genetic
Background
C57BL/6-Fem1atm1Seno
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fem1atm1Seno mutation (0 available); any Fem1a mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
digestive/alimentary system
• increased crypt loss after induction of colitis with DSS, also in DSS-treated wild-type and mutant recipients of mutant bone marrow
• significantly elevated accumulation of macrophages, neutrophils, B cells, CD4+ T cells and CD8+ T cells after induction of colitis with 2.5% dextran sodium sulfate (DSS)
• markedly higher levels of pro-inflammatory cytokines and chemokines such as Tnf, Il1b, Il6, Cxcl1 and Ccl2/Mcp1 after induction of colitis with DSS
• increased number of polyps at 63 days after treatment with polyp-inducing azoxymethane (AOM) and colitis-inducing dextran sodium sulfate (DSS), also in AOM+DSS-treated wild-type and mutant recipients of mutant bone marrow
• more Ki-67-positive cells and fewer apoptotic cells in tumors after AOM+DSS-treatment
• after induction of colitis with DSS
• more Ki-67-positive cells and fewer apoptotic cells in tumors after AOM+DSS-treatment
• after induction with 2.5% dextran sodium sulfate (DSS) and compared to DSS-treated wild-type mice
• higher mortality
• lower body weight
• reduced colon length, also in DSS-treated wild-type and mutant recipients of mutant bone marrow
• significantly elevated accumulation of macrophages, neutrophils, B cells, CD4+ T cells and CD8+ T cells, also in DSS-treated wild-type and mutant recipients of mutant bone marrow
• markedly higher levels of pro-inflammatory cytokines and chemokines such as Tnf, Il1b, Il6, Cxcl1 and Ccl2/Mcp1
• increased histological damage score, also in DSS-treated wild-type and mutant recipients of mutant bone marrow

endocrine/exocrine glands
• increased crypt loss after induction of colitis with DSS, also in DSS-treated wild-type and mutant recipients of mutant bone marrow

growth/size/body
• after induction of colitis with DSS

immune system
• after induction with 2.5% dextran sodium sulfate (DSS) and compared to DSS-treated wild-type mice
• higher mortality
• lower body weight
• reduced colon length, also in DSS-treated wild-type and mutant recipients of mutant bone marrow
• significantly elevated accumulation of macrophages, neutrophils, B cells, CD4+ T cells and CD8+ T cells, also in DSS-treated wild-type and mutant recipients of mutant bone marrow
• markedly higher levels of pro-inflammatory cytokines and chemokines such as Tnf, Il1b, Il6, Cxcl1 and Ccl2/Mcp1
• increased histological damage score, also in DSS-treated wild-type and mutant recipients of mutant bone marrow

mortality/aging
N
• viable

neoplasm
• more Ki-67-positive cells and fewer apoptotic cells in tumors after AOM+DSS-treatment

reproductive system





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