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Phenotypes Associated with This Genotype
Genotype
MGI:3582618
Allelic
Composition
Rb1tm1Tyj/Rb1+
Rbl1tm1Tyj/Rbl1+
Genetic
Background
involves: 129S2/SvPas * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rb1tm1Tyj mutation (5 available); any Rb1 mutation (111 available)
Rbl1tm1Tyj mutation (1 available); any Rbl1 mutation (60 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• similar to Rb1tm1Tyj heterozygotes, mice heterozygous for both Rb1tm1Tyj and Rbl1tm1Tyj die from tumors in the intermediate lobe of the pituitary gland at ~12 months of age

neoplasm
• double heterozygotes develop large pituitary tumors of the intermediate lobe that are comparable to those arising in single Rb1tm1Tyj heterozygotes with respect to both incidence and size
• such pituitary tumors are shown to arise from cells in which the wild-type allele of Rb1 is absent, whereas the wild-type allele of Rbl1 is retained

endocrine/exocrine glands
• double heterozygotes develop large pituitary tumors of the intermediate lobe that are comparable to those arising in single Rb1tm1Tyj heterozygotes with respect to both incidence and size
• such pituitary tumors are shown to arise from cells in which the wild-type allele of Rb1 is absent, whereas the wild-type allele of Rbl1 is retained

nervous system
• double heterozygotes develop large pituitary tumors of the intermediate lobe that are comparable to those arising in single Rb1tm1Tyj heterozygotes with respect to both incidence and size
• such pituitary tumors are shown to arise from cells in which the wild-type allele of Rb1 is absent, whereas the wild-type allele of Rbl1 is retained


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
12/10/2024
MGI 6.24
The Jackson Laboratory