About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rcbtb2tm1.1Xyw
targeted mutation 1.1, Xiao-Yan Wen
MGI:6431098
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rcbtb2tm1.1Xyw/Rcbtb2tm1.1Xyw involves: C57BL/6 * CBA MGI:6431136
ht2
Rcbtb2tm1.1Xyw/Rcbtb2+ involves: C57BL/6 * CBA MGI:6431137


Genotype
MGI:6431136
hm1
Allelic
Composition
Rcbtb2tm1.1Xyw/Rcbtb2tm1.1Xyw
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rcbtb2tm1.1Xyw mutation (0 available); any Rcbtb2 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• tumors are most commonly seen in the spleen, mesenteric lymph nodes, liver, and intestines
• tumors are present in 20 of 25 mice at 18-26 months of age compared to 5 of 19 wild-type controls
• tumors in the lower gastrointestinal tract often lead to destruction of the mucosal surface
• some mice have histiocyte-associated lymphoma or B cell lymphoma co-occurring with histiocytic sarcoma
• tumor cell morphology is frequently consistent with malignant histiocytes, although in some mice tumors have a plasma cell appearance

hematopoietic system
• frequently enlarged due to proliferation of transformed cells
• cells from 8-12 week old mice display enhanced viability in response to LPS in culture
• splenocytes from 8-12 week old mice display enhanced viability in response to LPS in culture

immune system
• frequently enlarged due to proliferation of transformed cells
• splenocytes from 8-12 week old mice display enhanced viability in response to LPS in culture
• frequently enlarged due to proliferation of transformed cells

liver/biliary system

digestive/alimentary system
• tumors in the lower gastrointestinal tract often lead to destruction of the mucosal surface

growth/size/body
• frequently enlarged due to proliferation of transformed cells

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
malignant histiocytic disease DOID:2570 J:282928




Genotype
MGI:6431137
ht2
Allelic
Composition
Rcbtb2tm1.1Xyw/Rcbtb2+
Genetic
Background
involves: C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rcbtb2tm1.1Xyw mutation (0 available); any Rcbtb2 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• tumors are present in 10 of 18 mice at 18-26 months of age compared to 5 of 19 wild-type controls
• tumors are most commonly seen in the spleen, mesenteric lymph nodes, liver, and intestines
• mice typically have multiple tumor bearing organs
• tumors in the lower gastrointestinal tract often lead to destruction of the mucosal surface
• some mice have histiocyte-associated lymphoma or B cell lymphoma co-occurring with histiocytic sarcoma
• tumor cell morphology is frequently consistent with malignant histiocytes, although in some mice tumors have a plasma cell appearance

hematopoietic system
• frequently enlarged due to proliferation of transformed cells

immune system
• frequently enlarged due to proliferation of transformed cells
• frequently enlarged due to proliferation of transformed cells

liver/biliary system

digestive/alimentary system
• tumors in the lower gastrointestinal tract often lead to destruction of the mucosal surface

growth/size/body
• frequently enlarged due to proliferation of transformed cells

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
malignant histiocytic disease DOID:2570 J:282928





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
11/05/2024
MGI 6.24
The Jackson Laboratory