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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Podxltm1Kmn
targeted mutation 1, Kelly M McNagny
MGI:2182833
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Podxltm1Kmn/Podxltm1Kmn either: (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlsHsd * C57BL/6) MGI:3041080
ht2
Podxltm1Kmn/Podxl+ either: (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlsHsd * C57BL/6) MGI:5811910


Genotype
MGI:3041080
hm1
Allelic
Composition
Podxltm1Kmn/Podxltm1Kmn
Genetic
Background
either: (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlsHsd * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Podxltm1Kmn mutation (0 available); any Podxl mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Edema in Podxltm1Kmn/Podxltm1Kmn mice

mortality/aging
• homozygotes die within 24 hours of birth

homeostasis/metabolism
• mild to severe edema after E15 in about 25% of homozygotes
• edema usually appears as subdermal swelling as early as E15 and a mildly turgid trunk and appendages at E18

growth/size/body
• ~30% of mice are born with an omphalocele or herniation of the gut into the umbilical cord
• 13 or 14 of embryos exhibit omphalocele up to E17, unlike wild-type embryos which show complete resolution of physiologic omphalocele by E15 or E16; ~70% of these mice resolve the omphalocele prior to birth

renal/urinary system
• lack foot processes
• lack slit diaphragms
• newborn mice lack urine in the bladder

cardiovascular system
• measured in embryos as a 15 fold increase in RBC released from a severed umbilical artery as compared to control embryos




Genotype
MGI:5811910
ht2
Allelic
Composition
Podxltm1Kmn/Podxl+
Genetic
Background
either: (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlsHsd * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Podxltm1Kmn mutation (0 available); any Podxl mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• 8 of 35 mice exhibit omphalocele at E17, indicating a delay in physiologic omphalocele resolution in utero





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