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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Wasltm2Sbs
targeted mutation 2, Scott B Snapper
MGI:3760279
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Wasltm2Sbs/Wasltm2Sbs
Six2tm1(tTA,tetO-EGFP/cre)Amc/Six2+
involves: 129 * C57BL/6J MGI:5486305
cn2
Wastm1Sbs/Wastm1Sbs
Wasltm2Sbs/Wasltm2Sbs
Tg(Lck-cre)1Cwi/?
involves: 129S6/SvEvTac * C57BL/6 MGI:3760284


Genotype
MGI:5486305
cn1
Allelic
Composition
Wasltm2Sbs/Wasltm2Sbs
Six2tm1(tTA,tetO-EGFP/cre)Amc/Six2+
Genetic
Background
involves: 129 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Six2tm1(tTA,tetO-EGFP/cre)Amc mutation (0 available); any Six2 mutation (16 available)
Wasltm2Sbs mutation (0 available); any Wasl mutation (39 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Hypoplasia and loss of glomeruli and proximal tubules in Wasltm2Sbs/Wasltm2Sbs Six2tm1(tTA,tetO-EGFP/cre)Amc/Six2+ kidneys

renal/urinary system
• decrease in proximal tubule numbers at P0




Genotype
MGI:3760284
cn2
Allelic
Composition
Wastm1Sbs/Wastm1Sbs
Wasltm2Sbs/Wasltm2Sbs
Tg(Lck-cre)1Cwi/?
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Lck-cre)1Cwi mutation (3 available)
Wasltm2Sbs mutation (0 available); any Wasl mutation (39 available)
Wastm1Sbs mutation (2 available); any Was mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• most mice develop signs of colitis by 2 months of age with elongation of crypts and mucosal thickening
• unlike wild-type thymocytes, single positive (SP) thymocytes fail to proliferate after CD3 stimulation
• spreading of TCRhigh CD4 or CD8 SP thymocytes on a surface covered with antibodies to CD3 and CD28 is reduced
• migratory responses to CCL19 or CXCL12 are reduced even more than in Wastm1Sbs homozygotes and compared to in wild-type cells
• mice exhibit a reduction in large and cycling double negative 3 (DN3) cells and, to a lesser degree, DN4 cells
• the ratio of DN3 to DN4 is skewed (3.18+/-1.89 compared to 0.74+/-0.45 in wild-type mice and 1.49+/-0.90 in Wastm1Sbs homozygotes)
• the percent of double positive (DP) CD69hi cells is greater than in wild-type
• the numbers of CD4+ and CD8+ T lymphocytes is reduced
• the number of thymocytes is reduced
• however, there is no increase in apoptosis
• mice have fewer single positive CD69hi cells compared to in wild-type mice and Wastm1Sbs homozygotes
• the number of single positive CD69low CD62Llow cells is increased compared to in wild-type mice

hematopoietic system
• unlike wild-type thymocytes, single positive (SP) thymocytes fail to proliferate after CD3 stimulation
• spreading of TCRhigh CD4 or CD8 SP thymocytes on a surface covered with antibodies to CD3 and CD28 is reduced
• migratory responses to CCL19 or CXCL12 are reduced even more than in Wastm1Sbs homozygotes and compared to in wild-type cells
• mice exhibit a reduction in large and cycling double negative 3 (DN3) cells and, to a lesser degree, DN4 cells
• the ratio of DN3 to DN4 is skewed (3.18+/-1.89 compared to 0.74+/-0.45 in wild-type mice and 1.49+/-0.90 in Wastm1Sbs homozygotes)
• the percent of double positive (DP) CD69hi cells is greater than in wild-type
• the numbers of CD4+ and CD8+ T lymphocytes is reduced
• the number of thymocytes is reduced
• however, there is no increase in apoptosis
• mice have fewer single positive CD69hi cells compared to in wild-type mice and Wastm1Sbs homozygotes
• the number of single positive CD69low CD62Llow cells is increased compared to in wild-type mice

digestive/alimentary system
• most mice develop signs of colitis by 2 months of age with elongation of crypts and mucosal thickening
• most mice develop signs of colitis by 2 months of age with elongation of crypts and mucosal thickening

endocrine/exocrine glands
• most mice develop signs of colitis by 2 months of age with elongation of crypts and mucosal thickening
• the number of thymocytes is reduced
• however, there is no increase in apoptosis
• unlike wild-type thymocytes, single positive (SP) thymocytes fail to proliferate after CD3 stimulation
• spreading of TCRhigh CD4 or CD8 SP thymocytes on a surface covered with antibodies to CD3 and CD28 is reduced
• migratory responses to CCL19 or CXCL12 are reduced even more than in Wastm1Sbs homozygotes and compared to in wild-type cells





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory