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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Arhgdiatm1Ytk
targeted mutation 1, Yoshimi Takai
MGI:3613573
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Arhgdiatm1Ytk/Arhgdiatm1Ytk involves: 129S/SvEv * C57BL/6 * DBA MGI:3614391
cx2
Arhgdiatm1Ytk/Arhgdiatm1Ytk
Arhgdibtm1Miyo/Arhgdibtm1Miyo
involves: 129S/SvEv MGI:3814726


Genotype
MGI:3614391
hm1
Allelic
Composition
Arhgdiatm1Ytk/Arhgdiatm1Ytk
Genetic
Background
involves: 129S/SvEv * C57BL/6 * DBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Arhgdiatm1Ytk mutation (0 available); any Arhgdia mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• reduced number of germ cells; no spermatids or spermatocytes are seen in the most extreme cases
• mature sperm are rarely seen
• mesangial cells are decreased in number

mortality/aging
• animals die within a year from renal failure

renal/urinary system
• capillary loop structure is destroyed
• endotheial cells are decreased in number
• kidney cysts present in proximal and distal renal tubules
• cystic dilation, with distal and collecting tubules more severely affected
• severe abnormalities or absent when nothing but cellular debris present
• absent when nothing but cellular debris present
• mesangial region is occupied by electron dense material
• mesangial cells are decreased in number
• sclerosis apparent in the mesangial region and some glomeruli exhibit globular sclerosis
• renal tubule epithelial cells are flattened and frequently delaminated from the basal membrane
• epithelial cells exhibit vacuolar degeneration predominantly at the basal side
• distal tubules contained debris consisting of acellular and amorphous casts
• epithelial cells of distal tubules show variable anomalies from nearly normal appearance in intact tubules to flattened and degenerating cells in dilated tubules
• cystic dilation, with distal and collecting tubules more severely affected
• distal tubules contained debris consisting of acellular and amorphous casts
• urinary protein concentrations at 6, 9 and 12 weeks of age are significantly increased compared to controls
• at 9 months of age, the proteinuria is severe indicating a progressive severity with age
• interstitial infiltration of inflammatory cells is observed
• reduced clearance at 12 weeks of age, indicating a defect in glomerular function
• at 12 weeks of age, levels of urine output are similar to controls
• at 9 months of age, severe polyuria is seen

growth/size/body
• kidney cysts present in proximal and distal renal tubules

homeostasis/metabolism
• 2 fold increase at 12 weeks of age and high levels are seen at 9 months of age
• at 9 months of age, serum urea nitrogen levels are approximately 8 fold higher than controls
• 1.5 fold increase at 12 weeks of age
• severly increased levels at 9 months of age (approximately 27 fold increase)
• normal serum albumin levels are seen at 12 weeks of age
• at 9 months of age, serum albumin levels are less than half that of controls
• urinary protein concentrations at 6, 9 and 12 weeks of age are significantly increased compared to controls
• at 9 months of age, the proteinuria is severe indicating a progressive severity with age

reproductive system
N
• in males, Leydig cells appear morphologically and functionally normal as well as ventral prostates and seminal vesicles
• in females, ovary histology is normal and the formation of secondary follicles and Graafian follicles is normal
• reduced number of germ cells; no spermatids or spermatocytes are seen in the most extreme cases
• mature sperm are rarely seen
• most tubules contained vacuoles to various degrees and the diameters of the tubules are smaller than in controls
• upon superovulation, homozygous females produce smaller numbers of eggs compared to controls
• in vitro fertilization studies show that homozygous embryos implant normally in pseudopregnant control mice, suggesting that the partial infertility of homozygous females is due to an intrinsic defect in the postimplantation reproductive development of homozygous females
• females produced few litters, and these consist of only one to three pups
• males are sterile with the exception of one litter produced
• in vitro fertilization experiments indicate that sperm from homozygous mice fertilized fewer eggs than control sperm

immune system
• there is a 44% reduction in the number of circulating T cells found in adults
• interstitial infiltration of inflammatory cells is observed

endocrine/exocrine glands
• most tubules contained vacuoles to various degrees and the diameters of the tubules are smaller than in controls

behavior/neurological
• while young homozygous mice are grossly normal, physical weakness and fraility are apparent with increasing age

hematopoietic system
• there is a 44% reduction in the number of circulating T cells found in adults

cardiovascular system
• capillary loop structure is destroyed
• endotheial cells are decreased in number

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
nephrotic syndrome DOID:1184 J:57995




Genotype
MGI:3814726
cx2
Allelic
Composition
Arhgdiatm1Ytk/Arhgdiatm1Ytk
Arhgdibtm1Miyo/Arhgdibtm1Miyo
Genetic
Background
involves: 129S/SvEv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Arhgdiatm1Ytk mutation (0 available); any Arhgdia mutation (18 available)
Arhgdibtm1Miyo mutation (0 available); any Arhgdib mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• though 75% of mice die during embryogenesis, mice born live at least until 12 months of age
• 75% of mice die during embryogenesis

immune system
• splenic B cells have a slightly enhanced migratory response to the chemokine CXCL12
• B cells activated in vitro with LPS have significantly higher proliferation rates
• mature CD4+ T cells accumulate in the medulla of the thymus
• immature B cells numbers are reduced by almost half in the bone marrow of adult mice
• newly formed B cells are reduced by 20-30% in the spleen of adult mice
• T1 and T2 transitional B cells are reduced by 20-30% in the spleen of adult mice
• the proportion of eosinophils in the bone marrow is three times higher than in controls
• increased numbers of eosinophils are also observed in the lung
• these increase numbers correlate with an increased amount of circulating IL-5
• these eosinophil differences are more clearly observed between the 12- to 55-wk-old groups than between the 6- and 11-wk-old groups
• mature B cell numbers are reduced by more than half in the bone marrow of adult mice
• follicular B cells are reduced by 20-30% in the spleen of adult mice
• MZ B cells are virtually absent in the spleen of adult mice
• pre-B cell numbers are reduced in the bone marrow to varying degrees depending on age
• numbers are reduced by about 25% at 7 weeks of age and by over 50% at 12-32 weeks of age
• there is a 80-90% reduction in the number of circulating T cells found in adults
• the percentage of double-positive thymocytes is reduced by 30% compared to controls at 18 weeks of age
• the percentages of single-positive thymocytes are increased 2-fold
• spleen cellularity is reduced in these mice
• localization of B cells is disorganized in the border region of the white pulp
• splenic T cells have reduced migratory responses to CXCL12, CCL21, and CCL19
• T cells activated in vitro have significantly less proliferation than controls
• the average serum concentrations of IL-5 (17 pg/ml vs 4.5 pg/ml in WT) are significantly increased
• while reduced B cells are found throughout the rest of the body, mesenteric lymph nodes have 2- to 3- fold increased numbers of B cells
• there are increases in the size and cellular densities of B cell follicles within the mesenteric lymph nodes

endocrine/exocrine glands
• mature CD4+ T cells accumulate in the medulla of the thymus
• testes showed drastic testicular degeneration

hematopoietic system
• splenic B cells have a slightly enhanced migratory response to the chemokine CXCL12
• B cells activated in vitro with LPS have significantly higher proliferation rates
• mature CD4+ T cells accumulate in the medulla of the thymus
• immature B cells numbers are reduced by almost half in the bone marrow of adult mice
• newly formed B cells are reduced by 20-30% in the spleen of adult mice
• T1 and T2 transitional B cells are reduced by 20-30% in the spleen of adult mice
• the proportion of eosinophils in the bone marrow is three times higher than in controls
• increased numbers of eosinophils are also observed in the lung
• these increase numbers correlate with an increased amount of circulating IL-5
• these eosinophil differences are more clearly observed between the 12- to 55-wk-old groups than between the 6- and 11-wk-old groups
• mature B cell numbers are reduced by more than half in the bone marrow of adult mice
• follicular B cells are reduced by 20-30% in the spleen of adult mice
• MZ B cells are virtually absent in the spleen of adult mice
• pre-B cell numbers are reduced in the bone marrow to varying degrees depending on age
• numbers are reduced by about 25% at 7 weeks of age and by over 50% at 12-32 weeks of age
• there is a 80-90% reduction in the number of circulating T cells found in adults
• the percentage of double-positive thymocytes is reduced by 30% compared to controls at 18 weeks of age
• the percentages of single-positive thymocytes are increased 2-fold
• spleen cellularity is reduced in these mice
• localization of B cells is disorganized in the border region of the white pulp
• splenic T cells have reduced migratory responses to CXCL12, CCL21, and CCL19
• T cells activated in vitro have significantly less proliferation than controls

homeostasis/metabolism
• the average serum concentrations of IL-5 (17 pg/ml vs 4.5 pg/ml in WT) are significantly increased

reproductive system
• testes showed drastic testicular degeneration
• male mice are totally sterile

cellular
• splenic B cells have a slightly enhanced migratory response to the chemokine CXCL12
• B cells activated in vitro with LPS have significantly higher proliferation rates
• T cells activated in vitro have significantly less proliferation than controls





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