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Phenotypes Associated with This Genotype
Genotype
MGI:4358554
Allelic
Composition
Kittm3.1Bsm/Kittm3.1Bsm
Genetic
Background
B6.129S1-Kittm3.1Bsm
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kittm3.1Bsm mutation (0 available); any Kit mutation (175 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice treated with a myelosuppressive dose of 5-fluorouracil (5-FU) die between 6 and 16 days post-treatment unlike similarly treated wild-type mice

hematopoietic system
• following phenylhydrazine (PHZ)- or 5-fluorouracil (5-FU)-induced anemia, stress-induced erythropoiesis is defective compared to in wild-type mice
• the ratio of Kit+ to Kit- proerythroblasts is decreased while the frequencies of Kit- erythroblasts is increased compared to in wild-type mice
• proerythroblast exhibit decreased proliferation and survival capacities compared to in wild-type mice
• following treatment with phenylhydrazine (PHZ), mice exhibit decreased frequency of bone marrow erythroid cells compared with similarly treated wild-type mice
• mice exhibit a 2-fold increase in KitnegCD71high erythroblasts compared with wild-type mice
• following treatment with EPO, red cell levels at 6 and 9 days are deficient compared to in similarly treated wild-type mice
• following treatment with a myelosuppressive dose of 5-fluorouracil (5-FU), hematocrit levels fall markedly prior to death between 6 and 16 days post-treatment unlike in similarly treated wild-type mice
• following treatment with a standard dose of 5-FU mice exhibit decreased hematocrit levels compared with similarly treated wild-type mice
• following treatment with phenylhydrazine (PHZ), mice exhibit deficient hematocrits compared with similarly treated wild-type mice
• during recovery from a standard dose of 5-fluorouracil (5-FU) compared to in similarly treated wild-type mice
• following treatment with phenylhydrazine (PHZ)

homeostasis/metabolism
• following treatment with EPO, red cell levels at 6 and 9 days are deficient compared to in similarly treated wild-type mice
• mice treated with a myelosuppressive dose of 5-fluorouracil (5-FU) die between 6 and 16 days post-treatment unlike similarly treated wild-type mice
• following treatment with a myelosuppressive dose of 5-fluorouracil (5-FU), mice fail to develop splenomegaly and exhibit reduced erythroblasts and hematocrit levels fall markedly prior to death between 6 and 16 days post-treatment unlike in similarly treated wild-type mice
• following treatment with a standard dose of 5-FU mice exhibit decreased hematocrit levels, red blood cell counts, and delayed recovery compared with similarly treated wild-type mice
• erythrocyte mean cell volume is increased during recovery from a standard dose of 5-fluorouracil (5-FU) compared to in similarly treated wild-type mice
• following treatment with phenylhydrazine (PHZ), mice exhibit decreased erythropoiesis, delayed recovery, deficient hematocrits, decreased spleen cellularity, a 10-fold decrease in splenic erythroblasts, and decreased bone marrow erythroid cells compared with similarly treated wild-type mice

immune system
• following treatment with phenylhydrazine (PHZ)


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
01/28/2026
MGI 6.24
The Jackson Laboratory