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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gt(ROSA)26Sortm2(H1/tetO-RNAi:Kdm1a)Arte
targeted mutation 2, TaconicArtemis
MGI:5468804
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Gt(ROSA)26Sortm2(H1/tetO-RNAi:Kdm1a)Arte/Gt(ROSA)26Sor+ involves: C57BL/6 MGI:5469737


Genotype
MGI:5469737
ht1
Allelic
Composition
Gt(ROSA)26Sortm2(H1/tetO-RNAi:Kdm1a)Arte/Gt(ROSA)26Sor+
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm2(H1/tetO-RNAi:Kdm1a)Arte mutation (0 available); any Gt(ROSA)26Sor mutation (942 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
N
• following withdrawal of doxycycline, peripheral blood parameters are normalized
• perturbed terminal granulopoiesis with a 2-fold increase in granulo-monocytic progenitors in doxycycline-treated mice
• increased proliferation and reduced quiescent cells in doxycycline-treated mice
• in doxycycline-treated mice
• expanded early but inhibited terminal erythropoiesis in doxycycline-treated mice
• splenic stress erythropoiesis with insufficient terminal erythropoiesis doxycycline-treated mice
• in doxycycline-treated mice
• expansion of pre-megakaryoerythroid progenitors in doxycycline-treated mice
• enhanced monopoiesis with a 3-fold increase in monocyte/dendritic progenitors in doxycycline-treated mice
• dysmorphic with marginalized hyperlobulated nuclei and reduced cytoplasmic volume in doxycycline-treated mice
• 7-fold in the bone marrow of doxycycline-treated mice
• reduction in marrow erythroid precursors in doxycycline-treated mice
• expansion of pre-erythroid colony-forming unit progenitors and colony forming unit erythroid in doxycycline-treated mice
• expanded in doxycycline-treated mice
• expansion of proerythroblasts in doxycycline-treated mice
• fewer large in doxycycline-treated mice
• in doxycycline-treated mice
• slightly in doxycycline-treated mice
• in doxycycline-treated mice
• however, bone marrow cellularity is normal

cellular
• perturbed terminal granulopoiesis with a 2-fold increase in granulo-monocytic progenitors in doxycycline-treated mice
• enhanced monopoiesis with a 3-fold increase in monocyte/dendritic progenitors in doxycycline-treated mice
• increased proliferation and reduced quiescent cells in doxycycline-treated mice

homeostasis/metabolism
• 7-fold in doxycycline-treated mice

immune system
• perturbed terminal granulopoiesis with a 2-fold increase in granulo-monocytic progenitors in doxycycline-treated mice
• enhanced monopoiesis with a 3-fold increase in monocyte/dendritic progenitors in doxycycline-treated mice
• in doxycycline-treated mice
• slightly in doxycycline-treated mice

growth/size/body
• in doxycycline-treated mice





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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
04/23/2024
MGI 6.23
The Jackson Laboratory