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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tom1l2Gt(XG909)Byg
gene trap XG909, BayGenomics
MGI:3784979
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Tom1l2Gt(XG909)Byg/Tom1l2Gt(XG909)Byg involves: 129P2/OlaHsd * C57BL/6J MGI:3790510
ht2
Tom1l2Gt(XG909)Byg/Tom1l2+ involves: 129P2/OlaHsd * C57BL/6J MGI:3790600


Genotype
MGI:3790510
hm1
Allelic
Composition
Tom1l2Gt(XG909)Byg/Tom1l2Gt(XG909)Byg
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tom1l2Gt(XG909)Byg mutation (1 available); any Tom1l2 mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Splenomegaly in Tom1l2Gt(XG909)Byg/Tom1l2Gt(XG909)Byg mice

behavior/neurological
• homozygotes show significantly increased freezing response

immune system
• a trend towards an increased number of nucleated cells (leukocytes) in the spleen is seen at both 7 weeks of age and 6 months of age
• lymph nodes exhibit a higher percentage of B cells in both older and younger mice
• lymph nodes exhibit a higher percentage of T cells in older mice
• spleens from 6 month old mutants show an increase in the percentage of CD4+ helper T cells
• spleens from 6 month old mutants show an increase in the percentage of CD8+ cytotoxic T cells
• 4 of 6 mutants exhibit larger, darker, abnormally shaped spleens
• splenomegaly is seen in homozygotes older than 1 year of age, with weights from 1.5 to 2 times normal
• within the white pulp, follicles (B-cell enriched regions) have increased cellularity
• within the white pulp, the periarteriolar lymphoid sheath (T-cell enriched regions) has increased cellularity
• a trend towards an increased number of nucleated cells (leukocytes) in the spleen is seen at both 7 weeks of age and 6 months of age
• spleens from 6 month old mutants show a decrease in the percentage of macrophages
• lymph nodes exhibit higher percentages of B cells and T cells in older mice and B cells in younger mice
• mutants exhibit a reduced humoral immune response; the IgM antibody-forming cell response to T-dependent antigen sheep RBC is decreased
• mutants exhibit severe inflammatory lesions when housed in woodchip bedding; if mutants are transferred to cages with corncob beddings, infections are less severe and less frequent
• infections include bronchopneumonia (2% incidence) and myocplasmosis (1% incidence)
• 15-20% incidence of skin/eye infections
• mutants show staphylococucus aureus infection

hematopoietic system
• lower platelet counts
• however, mutants are not anemic
• a trend towards an increased number of nucleated cells (leukocytes) in the spleen is seen at both 7 weeks of age and 6 months of age
• lymph nodes exhibit a higher percentage of B cells in both older and younger mice
• lymph nodes exhibit a higher percentage of T cells in older mice
• spleens from 6 month old mutants show an increase in the percentage of CD4+ helper T cells
• spleens from 6 month old mutants show an increase in the percentage of CD8+ cytotoxic T cells
• 4 of 6 mutants exhibit larger, darker, abnormally shaped spleens
• splenomegaly is seen in homozygotes older than 1 year of age, with weights from 1.5 to 2 times normal
• within the white pulp, follicles (B-cell enriched regions) have increased cellularity
• within the white pulp, the periarteriolar lymphoid sheath (T-cell enriched regions) has increased cellularity
• a trend towards an increased number of nucleated cells (leukocytes) in the spleen is seen at both 7 weeks of age and 6 months of age
• spleens from 6 month old mutants show a decrease in the percentage of macrophages

neoplasm
• metastatic neoplasia (renal adenocarcinoma with secondaries in the liver and lymph nodes)
• 20% of 9 month old or older mutants develop a variety of tumors within the lung, ovary, mammary gland, kidney, liver, prostate, abdomen, thorax, and skin
• tumor types range from primary and benign adenomas (pulmonary/brochoalveolar renal) to noninvasive or invasive neoplasms (basal cell carcinoma of the skin, liver, and renal adenocarcinoma, lymphoid hyperplasia, and tumors of the mammary gland, ovaries, and prostate) and metastatic neoplasia (renal adenocarcinoma with secondaries in the liver and lymph nodes)

vision/eye

cardiovascular system
• 9 month old mutants sometimes exhibit hemorrhagic bladder, hemorrhagic masses adjacent to spleen and ovary, and/or thoracic hemorrhage

craniofacial

renal/urinary system

skeleton

nervous system

integument
• hair loss resulting in bald patches
• gross inflammatory lesions of the skin

reproductive system

endocrine/exocrine glands

growth/size/body
• splenomegaly is seen in homozygotes older than 1 year of age, with weights from 1.5 to 2 times normal

respiratory system




Genotype
MGI:3790600
ht2
Allelic
Composition
Tom1l2Gt(XG909)Byg/Tom1l2+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tom1l2Gt(XG909)Byg mutation (1 available); any Tom1l2 mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• heterozygotes show increased freezing response
• heterozygotes show increased rearing behavior in the open field at 10, 20, and 30 weeks of age but not at 5 weeks
• a higher proportion of heterozygotes than wild-type exhibit wild running

immune system

hematopoietic system

neoplasm
• mutants exhibit a variety of tumors, including skin, lung, and kidney tumors, soft tissue mass in the vulva, lachrymal glad enlargement, ovarian cysts and dark mass on prostate

vision/eye
• corneal ulcers
• ocular assymmetry

adipose tissue
• 3% of mutants develop excess fat deposition in the abdomen

nervous system

respiratory system

skeleton

endocrine/exocrine glands

reproductive system

integument
• heterozygotes exhibit gross inflammatory lesions of the skin

growth/size/body





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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
04/16/2024
MGI 6.23
The Jackson Laboratory