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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Relatm2.1Gho
targeted mutation 2.1, Sankar Ghosh
MGI:4830882
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Relatm2.1Gho/Relatm2.1Gho involves: 129S6/SvEvTac * C57BL/6 MGI:4830883
cx2
Relatm2.1Gho/Relatm2.1Gho
Tnfrsf1atm1Mak/Tnfrsf1atm1Mak
involves: 129S2/SvPas * 129S6/SvEvTac MGI:5574110


Genotype
MGI:4830883
hm1
Allelic
Composition
Relatm2.1Gho/Relatm2.1Gho
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Relatm2.1Gho mutation (0 available); any Rela mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• typically die 8-20 d after birth

growth/size/body
• dramatically runted animals by P8-P10
• mice exhibit progressive growth retardation, beginning at postnatal day P4-P5

immune system
• immature and mature neutrophils on peripheral blood smear
• authors state spleen exhibits features similar to the liver
• systemic inflammation
• histiocytic inflammatory infiltrates
• multifocal suppurative and histiocytic interstitial and perivascular pneumonia

muscle

respiratory system
• multifocal suppurative and histiocytic interstitial and perivascular pneumonia

hematopoietic system
• extramedullary hematopoeisis with a predominance of myeloid and megakaryocytic cells
• immature and mature neutrophils on peripheral blood smear
• authors state spleen exhibits features similar to the liver

liver/biliary system
• histiocytic inflammatory infiltrates
• in rare aged mouse (3.5 months) liver is shrunken and distorted
• accompanied by dying hepatocytes
• in rare aged mouse (3.5 months) liver is distorted by bridging fibrosis extending from the capsule through the parenchyma, multifocal capsular fibrosis and lymphocytic inflammation that extended into underlying parenchyma are also seen

nervous system
• authors state brain exhibits features similar to the liver

cardiovascular system
• authors state heart exhibits features similar to the liver

digestive/alimentary system
• authors state colon exhibits features similar to the liver

skeleton
• authors state bone exhibits features similar to the liver

integument
• shortened distorted hair follicles
• suppurative dermatitis with dermal fibrosis and multifocal epidermal necrosis




Genotype
MGI:5574110
cx2
Allelic
Composition
Relatm2.1Gho/Relatm2.1Gho
Tnfrsf1atm1Mak/Tnfrsf1atm1Mak
Genetic
Background
involves: 129S2/SvPas * 129S6/SvEvTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Relatm2.1Gho mutation (0 available); any Rela mutation (28 available)
Tnfrsf1atm1Mak mutation (2 available); any Tnfrsf1a mutation (52 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 50%-60% die sometime between 1 and 6 months of age

vision/eye
• vascularized and proliferative corneal lesion developed in the central region of the cornea
• neutrophils and macrophages
• occasional dying keratinocytes are present
• severe corneal epithelial thickening is observed, occurring abruptly at the junction of the central and peripheral
• at 25 days, the corneal epithelium is slightly thinner and keratinocytes are less orderly

liver/biliary system
• slowly progressive hepatic inflammation
• Inflammatory foci are characterized by an increasing number of interstitial and perivascular macrophages with fewer neutrophils
• capsular fibrosis and inflammation is also seen

cardiovascular system
• vascularized and proliferative corneal lesion developed in the central region of the cornea

immune system
• neutrophils and macrophages
• slowly progressive hepatic inflammation
• Inflammatory foci are characterized by an increasing number of interstitial and perivascular macrophages with fewer neutrophils





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory