About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gadd45atm1Ajf
targeted mutation 1, Albert J Fornace
MGI:2182720
Summary 8 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Gadd45atm1Ajf/Gadd45atm1Ajf either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6) MGI:3618357
hm2
Gadd45atm1Ajf/Gadd45atm1Ajf either: (involves: 129P2/OlaHsd * C57BL/6 * SKH1) or (involves: 129X1/SvJ * C57BL/6 * SKH1) MGI:3618364
hm3
Gadd45atm1Ajf/Gadd45atm1Ajf involves: 129 MGI:4420762
cx4
Cdkn1atm1Led/Cdkn1atm1Led
Gadd45atm1Ajf/Gadd45atm1Ajf
either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6) MGI:3618363
cx5
Cdkn1atm1Tyj/Cdkn1atm1Tyj
Gadd45atm1Ajf/Gadd45atm1Ajf
either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ) MGI:4420763
cx6
Gadd45atm1Ajf/Gadd45atm1Ajf
Xpctm1Ecf/Xpctm1Ecf
either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129X1/SvJ * C57BL/6) MGI:3719353
cx7
Gadd45atm1Ajf/Gadd45atm1Ajf
Gadd45btm1Daa/Gadd45btm1Daa
Gadd45gtm1Mhol/Gadd45gtm1Mhol
either: (involves: 129X1/SvJ) or (involves: 129P2/OlaHsd * 129X1/SvJ) MGI:3653937
cx8
Brca1tm2.1Cxd/Brca1tm2.1Cxd
Gadd45atm1Ajf/Gadd45atm1Ajf
involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * C57BL/6 MGI:4360343


Genotype
MGI:3618357
hm1
Allelic
Composition
Gadd45atm1Ajf/Gadd45atm1Ajf
Genetic
Background
either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gadd45atm1Ajf mutation (2 available); any Gadd45a mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygous mice begin to die after 7 months of age and the median life span of females is reduced to 16 months compared to about 22 months for wild-type

cellular
• splenocytes and keratinocytes have 3 or more centrosomes per cell and many keratinocytes have asymmetric distribution of centrosomes during mitosis
• most MEFs with extra centrosomes also have large, partially cleaved, bilobed nuclei
• most MEFs with extra centrosomes also have large, partially cleaved, bilobed nuclei
• chromosomal aberrations including double minutes, centromere fusions or end associations, chromatid deletions, and incomplete triradials and quadraradials
• less than 40% of homozygous MEFs are diploid at passage 4 with the rest either tetraploid or aneuploid, unlike wild-type MEFs where about 70% of cells are diploid, 30% are tetraploid and no aneuploid cells are seen
• at passage 11 no homozygous MEFs are diploid and over 60% are aneuploid
• at passage 4 some aneuploid cells are seen and by passage 11 over 60% of cells are aneuploid
• about 2% of freshly isolated splenic lymphoblasts display aneuploidy while no aneuploid cells are found in wild-type mice
• diffuse global mesangial proliferation involving 40 - 100% of glomeruli is seen in older homozygotes
• in some glomeruli
• retroviral transfection of homozygous MEFs with an activated ras allele produces obvious transformed foci and these cells are able to form colonies in soft agar, unlike wild-type MEFs where the introduction of 2 activated oncogenes is needed for transformation
• the number of colonies produced in the soft agar assay is less than in transfected homozygous Trp53 null MEFs
• however, when exposed to ionizing radiation or UV apoptosis is similar to wild-type unlike Trp53 null MEFs
• some MEFs fail to fully condense all their chromatin at mitosis
• IR induces a strong G1 delay similar to wild-type cells and unlike in Cdkn1a null cells
• when exposed to UV the dose dependent reduction in the mitotic index is decreased compared to wild-type cells; however, when exposed to ionizing radiation (IR), the reduction in mitotic index is similar to wild-type and IR or UV-induced apoptosis is similar to wild-type unlike Trp53 null MEFs
• the sensitivity of primary T cell activation by anti-CD3 is increased with a 3- to 10-fold leftward shift in the dose-response curve and the maximal proliferative response is about 2-fold more than in wild-type cells
• however, proliferation in response to cytokines and T cell receptor independent proliferation is not increased compared to controls
• from passage 5-7 homozygous MEFs progressively grow more rapidly and attain higher saturation densities compared to wild-type cells; however at earlier passages growth is similar to wild-type
• low passage MEFs have a plating efficiency of about 0.025% compared to 0.005% in wild-type cells, 1.6% in Trp53 null cells, 1.2% in Cdkn1a null cells, and up to 1.4% in Gadd45a Cdkn1a double null cells
• diffuse global mesangial proliferation involving 40 - 100% of glomeruli is seen in older homozygotes

hematopoietic system
• the sensitivity of primary T cell activation by anti-CD3 is increased with a 3- to 10-fold leftward shift in the dose-response curve and the maximal proliferative response is about 2-fold more than in wild-type cells
• however, proliferation in response to cytokines and T cell receptor independent proliferation is not increased compared to controls
• thymus weight as a percent of body weight is increased about 70% compared to wild-type
• lymphoid hyperplasia is seen in the lymph nodes and spleen of 9 month old homozygotes
• increased apoptosis induced by UV, daunorubicin, or VP-16 is seen in bone marrow cells
• after UV chemotherapy or treatment with daunorubicin, or VP-16 homozygous bone marrow cells yield 6-fold or 8-16-fold, respectively, fewer IL-3 stimulated colonies compared to wild-type cells
• following treatment with UV or VP-16, but not daunorubicin, homozygous bone marrow cells fail to arrest at G2/M unlike wild-type cells
• the proportion of total T cells is increased in the spleen and lymph nodes compared to wild-type mice
• thymocyte number is increased but the distribution of thymocyte subpopulations is similar to wild-type
• at 7-9 months of age 47% of homozygous females are leukopenic compared to 7% of wild-type mice
• at 7-9 months of age 40% of homozygous females are lymphopenic compared to 7% of wild-type mice
• 2-fold increase in IgG1 and high levels of IgG2b and IgG3 anti-double stranded DNA antibodies at 7 - 9 months of age
• 2-fold increase in IgM at 7 - 9 months of age

immune system
• the sensitivity of primary T cell activation by anti-CD3 is increased with a 3- to 10-fold leftward shift in the dose-response curve and the maximal proliferative response is about 2-fold more than in wild-type cells
• however, proliferation in response to cytokines and T cell receptor independent proliferation is not increased compared to controls
• thymus weight as a percent of body weight is increased about 70% compared to wild-type
• lymphoid hyperplasia is seen in the lymph nodes and spleen of 9 month old homozygotes
• the proportion of total T cells is increased in the spleen and lymph nodes compared to wild-type mice
• thymocyte number is increased but the distribution of thymocyte subpopulations is similar to wild-type
• at 7-9 months of age 47% of homozygous females are leukopenic compared to 7% of wild-type mice
• at 7-9 months of age 40% of homozygous females are lymphopenic compared to 7% of wild-type mice
• 2-fold increase in IgG1 and high levels of IgG2b and IgG3 anti-double stranded DNA antibodies at 7 - 9 months of age
• 2-fold increase in IgM at 7 - 9 months of age
• after 7 months of age in female homozygotes the occurrence and titer of antibodies against double stranded DNA is increased compared to wild-type mice
• after 7 months of age in female homozygotes the occurrence and titer of antibodies against histones is increased compared to wild-type mice
• after 7 months of age in female homozygotes the occurrence and titer of antibodies against single stranded DNA is increased compared to wild-type mice
• lymphocytic infiltrates are seen in the lung and salivary glands at 9 months of age
• some glomeruli contain inflammatory cells, nuclear debris, and mesangial cell interposition, mild dilation of the proximal tubules occurs, and mild to severe dense perivascular mononuclear cell infiltrates are seen suggesting autoimmune glomerulonphritis

nervous system
• about 8% of pups from homozygous crosses display exencephaly

reproductive system
• about 50% of females fail to deliver their first litter resulting in death of the female

neoplasm
• following gamma irradiation tumor latency is decreased, frequency is increased, and most of the tumors are lymphomas of thymic origin

renal/urinary system
• diffuse global mesangial proliferation involving 40 - 100% of glomeruli is seen in older homozygotes
• in some glomeruli
• diffuse global mesangial proliferation involving 40 - 100% of glomeruli is seen in older homozygotes
• 150 +/- 50 mg/dl of protein is seen in the urine of homozygous females suggesting chronic nephropathy
• some glomeruli contain inflammatory cells, nuclear debris, and mesangial cell interposition, mild dilation of the proximal tubules occurs, and mild to severe dense perivascular mononuclear cell infiltrates are seen suggesting autoimmune glomerulonphritis
• mild dilation of the proximal tubules

homeostasis/metabolism
• 150 +/- 50 mg/dl of protein is seen in the urine of homozygous females suggesting chronic nephropathy

integument
• in newborn and adult homozygous mice acute UVB-induced epidermal apoptosis, erythema, and induction of subcorneal pustules or epidermal erosion is reduced
• after UVB irradiation homozygous primary keratinocytes show an attenuated G1 arrest and a more pronounced reduction in G2 arrest compared to wild-type cells; however UVB-induced G1 and G2 arrest in dermal fibroblasts is similar to wild-type

endocrine/exocrine glands
• thymus weight as a percent of body weight is increased about 70% compared to wild-type
• thymocyte number is increased but the distribution of thymocyte subpopulations is similar to wild-type




Genotype
MGI:3618364
hm2
Allelic
Composition
Gadd45atm1Ajf/Gadd45atm1Ajf
Genetic
Background
either: (involves: 129P2/OlaHsd * C57BL/6 * SKH1) or (involves: 129X1/SvJ * C57BL/6 * SKH1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gadd45atm1Ajf mutation (2 available); any Gadd45a mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• after1 year of UV exposure (3x per week) the number of proliferative epidermal lesions is increased and these include; pre-malignant atypical epidermal hyperplasia, squamous cell papillomas, and squamous cell carcinomas

integument
• after 1 year of UV exposure (3x per week) the number of proliferative epidermal lesions is increased




Genotype
MGI:4420762
hm3
Allelic
Composition
Gadd45atm1Ajf/Gadd45atm1Ajf
Genetic
Background
involves: 129
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gadd45atm1Ajf mutation (2 available); any Gadd45a mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• keratinocytes exposed to UV-irradiation exhibit defective nucleotide excision repair compared with similarly treated wild-type cells

homeostasis/metabolism
• keratinocytes exposed to UV-irradiation exhibit defective nucleotide excision repair compared with similarly treated wild-type cells




Genotype
MGI:3618363
cx4
Allelic
Composition
Cdkn1atm1Led/Cdkn1atm1Led
Gadd45atm1Ajf/Gadd45atm1Ajf
Genetic
Background
either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn1atm1Led mutation (1 available); any Cdkn1a mutation (63 available)
Gadd45atm1Ajf mutation (2 available); any Gadd45a mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• double homozygous mice begin to die after 4 months of age and the median life span of females and males is reduced to 10 and 8 months, respectively, compared to about 22 months for wild-type

cellular
• after 14 weeks of selection with L-aspartic acid, N-(phosphonoacetyl) (PALA, an assay for gene amplification) homozygous MEFs develop resistance to up to 500uM PALA unlike wild-type cells which do not develop resistance and 20-fold greater than the resistance seen in Cdkn1a single homozygous MEFs
• global mesangial proliferation involving 10 - 100% of glomeruli is seen in older double homozygotes
• in some glomeruli
• proliferation in response to cytokines is increased; however, T cell receptor independent proliferation is not increased compared to wild-type
• low passage MEFs have a plating efficiency of up to 1.4% compared to 0.005% in wild-type cells, 0.025% in Gadd45a null cells, 1.6% in Trp53 null cells, and 1.2% in Cdkn1a null cells
• global mesangial proliferation involving 10 - 100% of glomeruli is seen in older double homozygotes
• segmental glomerular endothelial cell proliferation is seen in older double homozygotes

immune system
• lymphoid hyperplasia is seen in the lymph nodes and spleen of 4 month old double homozygotes
• at 7-9 months of age 73% of double homozygous females are leukopenic compared to 7% of wild-type mice and 47% of Gadd45a single homozygous females
• at 7-9 months of age 53% of double homozygous females are lymphopenic compared to 7% of wild-type mice and 40% of Gadd45a single homozygous females
• at 7-9 months of age 46% of double homozygous males are lymphopenic
• 2-fold increase in IgG1 and high levels of IgG2b and IgG3 anti-double stranded DNA antibodies at 7 - 9 months of age
• 2-fold increase in IgM at 7 - 9 months of age
• the sensitivity of primary T cell activation is increased with a 3- to 10-fold leftward shift in the dose-response curve and the maximal proliferative response is about 2-fold more than in wild-type cells
• proliferation in response to cytokines is increased; however, T cell receptor independent proliferation is not increased compared to wild-type
• after 4 months of age in female and male double homozygotes the occurrence and titer of antibodies against double stranded DNA is increased compared to wild-type mice and single homozygous mice
• after 4 months of age in female and male double homozygotes the occurrence and titer of antibodies against histones is increased compared to wild-type mice and single homozygous mice
• after 4 months of age in female and male double homozygotes the occurrence and titer of antibodies against single stranded DNA is increased compared to wild-type mice and single homozygous mice
• lymphocytic infiltrates are seen in the lung and salivary glands at 4 months of age
• some glomeruli contain inflammatory cells, nuclear debris, and mesangial cell interposition, mild dilation of the proximal tubules occurs, and mild to severe dense perivascular mononuclear cell infiltrates are seen suggesting autoimmune glomerulonphritis

renal/urinary system
• segmental endothelial cell proliferation is seen in older double homozygotes
• global mesangial proliferation involving 10 - 100% of glomeruli is seen in older double homozygotes
• in some glomeruli
• global mesangial proliferation involving 10 - 100% of glomeruli is seen in older double homozygotes
• segmental glomerular endothelial cell proliferation is seen in older double homozygotes
• 220 +/- 40 mg/dl of protein is seen in the urine of double homozygous mice suggesting chronic nephropathy
• some glomeruli contain inflammatory cells, nuclear debris, and mesangial cell interposition, mild dilation of the proximal tubules occurs, and mild to severe dense perivascular mononuclear cell infiltrates are seen suggesting autoimmune glomerulonphritis
• mild dilation of the proximal tubules

homeostasis/metabolism
• 220 +/- 40 mg/dl of protein is seen in the urine of double homozygous mice suggesting chronic nephropathy

hematopoietic system
• lymphoid hyperplasia is seen in the lymph nodes and spleen of 4 month old double homozygotes
• at 7-9 months of age 73% of double homozygous females are leukopenic compared to 7% of wild-type mice and 47% of Gadd45a single homozygous females
• at 7-9 months of age 53% of double homozygous females are lymphopenic compared to 7% of wild-type mice and 40% of Gadd45a single homozygous females
• at 7-9 months of age 46% of double homozygous males are lymphopenic
• 2-fold increase in IgG1 and high levels of IgG2b and IgG3 anti-double stranded DNA antibodies at 7 - 9 months of age
• 2-fold increase in IgM at 7 - 9 months of age
• the sensitivity of primary T cell activation is increased with a 3- to 10-fold leftward shift in the dose-response curve and the maximal proliferative response is about 2-fold more than in wild-type cells
• proliferation in response to cytokines is increased; however, T cell receptor independent proliferation is not increased compared to wild-type

cardiovascular system
• segmental endothelial cell proliferation is seen in older double homozygotes




Genotype
MGI:4420763
cx5
Allelic
Composition
Cdkn1atm1Tyj/Cdkn1atm1Tyj
Gadd45atm1Ajf/Gadd45atm1Ajf
Genetic
Background
either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn1atm1Tyj mutation (3 available); any Cdkn1a mutation (63 available)
Gadd45atm1Ajf mutation (2 available); any Gadd45a mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• UV-irradiated keratinocytes do not undergo apoptosis unlike keratinocytes from Gadd45atm1Ajf homozygotes

homeostasis/metabolism
N
• UV-irradiated keratinocytes exhibit normal nucleotide excision repair




Genotype
MGI:3719353
cx6
Allelic
Composition
Gadd45atm1Ajf/Gadd45atm1Ajf
Xpctm1Ecf/Xpctm1Ecf
Genetic
Background
either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129X1/SvJ * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gadd45atm1Ajf mutation (2 available); any Gadd45a mutation (15 available)
Xpctm1Ecf mutation (1 available); any Xpc mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• at 24 months of age, only 28% of mutants are alive compared to 43% of wild-type

neoplasm
• some mutants exhibit malignant adenocarcinoma with metastasis to adjacent lymph nodes
• 100% of mutants develop lung tumors by 24 months of age; display a full range of lung lesions, ranging from mild atypia and hyperplasia to malignant adenocarcinoma with metastasis to adjacent lymph nodes
• majority of mutants develop lung adenocarcinomas coincident with adenomas

respiratory system
• 100% of mutants develop lung tumors by 24 months of age; display a full range of lung lesions, ranging from mild atypia and hyperplasia to malignant adenocarcinoma with metastasis to adjacent lymph nodes
• majority of mutants develop lung adenocarcinomas coincident with adenomas

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
lung cancer DOID:1324 OMIM:211980
OMIM:608935
OMIM:612571
OMIM:612593
OMIM:614210
J:101421




Genotype
MGI:3653937
cx7
Allelic
Composition
Gadd45atm1Ajf/Gadd45atm1Ajf
Gadd45btm1Daa/Gadd45btm1Daa
Gadd45gtm1Mhol/Gadd45gtm1Mhol
Genetic
Background
either: (involves: 129X1/SvJ) or (involves: 129P2/OlaHsd * 129X1/SvJ)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gadd45atm1Ajf mutation (2 available); any Gadd45a mutation (15 available)
Gadd45btm1Daa mutation (1 available); any Gadd45b mutation (12 available)
Gadd45gtm1Mhol mutation (0 available); any Gadd45g mutation (11 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• proliferation in the outer medullas of triple knockouts




Genotype
MGI:4360343
cx8
Allelic
Composition
Brca1tm2.1Cxd/Brca1tm2.1Cxd
Gadd45atm1Ajf/Gadd45atm1Ajf
Genetic
Background
involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Brca1tm2.1Cxd mutation (1 available); any Brca1 mutation (114 available)
Gadd45atm1Ajf mutation (2 available); any Gadd45a mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Exencephaly and growth retardation in Brca1tm2.1Cxd/Brca1tm2.1Cxd Gadd45atm1Ajf/Gadd45atm1Ajf embryos

mortality/aging
• no double homozygotes at birth
• embryos normal at E9.5-E10.5
• smaller than normal at E11.5 to E15.5 with many dying or dead

nervous system
• failure of anterior neural tube to close
• neuroepithelium of mutant brain fail to develop after E9.5
• higher rate of apoptosis in the neuroepithelium

cellular
• about 45% of MEFs have more than two centrosomes
• about 28% of cells in E9.5 embryos have more than two centrosomes
• about 40% of MEFs are aneuploid at passage 2

embryo

growth/size/body





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
12/10/2024
MGI 6.24
The Jackson Laboratory