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Phenotypes Associated with This Genotype
Genotype
MGI:3839787
Allelic
Composition
Cdkn1btm1Ako/Cdkn1btm1Ako
Genetic
Background
involves: 129S1/Sv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn1btm1Ako mutation (0 available); any Cdkn1b mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
adipose tissue
• 25% compared to in wild-type mice
• the number of adipocytes in the parametrial fat pad is increased 1.9-fold compared to in wild-type mice
• adipocyte hyperplasia is observed in small, medium, and large adipocytes
• the number of small adipocytes is increased 3-fold compared to in wild-type mice
• 80% at 130 days compared to in wild-type mice

respiratory system
• 8% of mice develop lung adenomas as solitary, uniform nodules with clear borders and homogeneous tumor cell type

neoplasm
• mice occasionally develop ovarian epithelial tumors
• 8% of mice develop lung adenomas as solitary, uniform nodules with clear borders and homogeneous tumor cell type

skeleton
• the total area of connective tissue islands in the junctional epithelium is larger than in wild-type mice

growth/size/body
• the total area of connective tissue islands in the junctional epithelium is larger than in wild-type mice
• at 60 to 120 days
• 37% compared to in wild-type mice

homeostasis/metabolism
• testosterone treatment increases the seminal vesicle weight more than in similarly treated wild-type mice

nervous system

renal/urinary system
• 37% compared to in wild-type mice

craniofacial
• the total area of connective tissue islands in the junctional epithelium is larger than in wild-type mice

endocrine/exocrine glands
• DNA content is increased 47% compared to in wild-type mice
• mice occasionally develop ovarian epithelial tumors
• ventral prostate and dorsolateral prostate epithelial proliferation is increased 2- and 3.8-fold, respectively, compared to in wild-type mice
• luminal epithelial apoptosis is increased 8.7-fold compared to in wild-type mice
• testosterone treatment does not alter increased luminal epithelial apoptosis rates

reproductive system
• DNA content is increased 47% compared to in wild-type mice
• mice occasionally develop ovarian epithelial tumors
• ventral prostate and dorsolateral prostate epithelial proliferation is increased 2- and 3.8-fold, respectively, compared to in wild-type mice
• luminal epithelial apoptosis is increased 8.7-fold compared to in wild-type mice
• testosterone treatment does not alter increased luminal epithelial apoptosis rates


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
01/06/2026
MGI 6.24
The Jackson Laboratory