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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tcf21tm1(cre)Seq
targeted mutation 1, Susan E Quaggin
MGI:5446790
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Ptch1tm1Bjw/Ptch1tm1Bjw
Tcf21tm1(cre)Seq/Tcf21+
involves: 129S1/Sv * 129T2/SvEms * 129X1/SvJ MGI:5446894
cn2
Ctnnb1tm1Mmt/Ctnnb1tm1Mmt
Tcf21tm1(cre)Seq/Tcf21+
involves: 129S1/Sv * 129X1/SvJ MGI:5446891
cn3
Ctnnb1tm2Kem/Ctnnb1tm2Kem
Tcf21tm1(cre)Seq/Tcf21+
involves: 129S1/Sv * 129X1/SvJ MGI:5446892


Genotype
MGI:5446894
cn1
Allelic
Composition
Ptch1tm1Bjw/Ptch1tm1Bjw
Tcf21tm1(cre)Seq/Tcf21+
Genetic
Background
involves: 129S1/Sv * 129T2/SvEms * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ptch1tm1Bjw mutation (2 available); any Ptch1 mutation (115 available)
Tcf21tm1(cre)Seq mutation (0 available); any Tcf21 mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos die at varying timepoints between E12.5 and birth

renal/urinary system
• kidneys are comparable in size to controls, display numerous abnormal phenotypes
• multiple cysts are observed, with some cysts containing glomeruli, with other cysts originating in the renal tubules
• cysts arise along entire nephron
• collecting ducts are dilated, distorted and winding, with increased cell proliferation in walls of cysts
• pelvic area is dilated

neoplasm
• lethality is suggested to result from an aggressive embryonic tumor with minimal renal invasion

growth/size/body
• multiple cysts are observed, with some cysts containing glomeruli, with other cysts originating in the renal tubules
• cysts arise along entire nephron




Genotype
MGI:5446891
cn2
Allelic
Composition
Ctnnb1tm1Mmt/Ctnnb1tm1Mmt
Tcf21tm1(cre)Seq/Tcf21+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctnnb1tm1Mmt mutation (0 available); any Ctnnb1 mutation (49 available)
Tcf21tm1(cre)Seq mutation (0 available); any Tcf21 mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mutants are born in expected numbers but die within hours of birth

renal/urinary system
• rudimentary kidneys are cystic with only a only a few immature glomeruli and show random disorganized nephrogenic aggregates at periphery
• about 20% of E18.5 embryos or neonatal pups exhibit hypoplastic rudimentary kidneys
• most kidneys show some degree of hypoplasia
• hydroureter with hypoplasia is observed at E18.5 and in PO pups with about 73.5% incidence; these kidneys also exhibit dilated tubules

growth/size/body
• rudimentary kidneys are cystic with only a only a few immature glomeruli and show random disorganized nephrogenic aggregates at periphery




Genotype
MGI:5446892
cn3
Allelic
Composition
Ctnnb1tm2Kem/Ctnnb1tm2Kem
Tcf21tm1(cre)Seq/Tcf21+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctnnb1tm2Kem mutation (1 available); any Ctnnb1 mutation (49 available)
Tcf21tm1(cre)Seq mutation (0 available); any Tcf21 mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos die between E12.5 and birth

renal/urinary system
• about 33% of mutants have hypoplastic/dysplastic kidneys with a few disorganized glomeruli
• most kidneys show some degree of hypoplasia
• at E18.5 about 66.5% of mutants display kidney fusion at the midline

neoplasm
• 100% of mutants display embryonic tumor affecting kidney, gut, heart, and lungs, which appears to arise from multiple mesenchymal tissues





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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
04/23/2024
MGI 6.23
The Jackson Laboratory