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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Urostm1Cged
targeted mutation 1, Cecile Ged
MGI:3619379
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Urostm1Cged/Urostm1Cged involves: 129S2/SvPas MGI:3621357


Genotype
MGI:3621357
hm1
Allelic
Composition
Urostm1Cged/Urostm1Cged
Genetic
Background
involves: 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Urostm1Cged mutation (1 available); any Uros mutation (18 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• teeth, liver, spleen, bones and kidneys are a reddish-brown color due to accumulation of porphyrins
• massive accumulation of porphyrins is found in the blood, urine, and feces
• red urine

hematopoietic system
• spleen is enlarged and has a brownish color due to accumulation of porphyrins
• high reticulocyte count and presence of many erythroblasts with poikilocytosis and anisochromia indicate ongoing hemolysis
• severe microcytic and hypochromic anemia
• increase in the number of erythroid precursor cells
• enlarged red pulp and increase in erythroid precursor cells

craniofacial

immune system
• spleen is enlarged and has a brownish color due to accumulation of porphyrins
• enlarged red pulp and increase in erythroid precursor cells

liver/biliary system
• liver is enlarged and a brownish color due to accumulation of porphyrins
• clusters of erythroid cells are associated with mild centrilobular steatosis

renal/urinary system
• red urine
• accumulation of eosinophilic material in the glomeruli
• accumulation of eosinophilic material in the tubules
• iron deposition in the epithelial layer of the proximal cortical tubules

skeleton
• bones are an intense reddish-brown color after removal of the bone marrow

growth/size/body
• hypotrophic at birth
• liver is enlarged and a brownish color due to accumulation of porphyrins
• spleen is enlarged and has a brownish color due to accumulation of porphyrins

integument
• photosensitive lesions are seen on the ears and back of the neck

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
cutaneous porphyria DOID:13271 OMIM:263700
J:105776





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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