Symbol Name ID |
Cyp1a2
cytochrome P450, family 1, subfamily a, polypeptide 2 MGI:88589 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal erythrocyte enzyme concentration or activity |
Increased circulating iron concentration |
Abnormal circulating porphyrin concentration |
Increased circulating ferritin concentration |
Decreased circulating hepcidin concentration |
Abnormal circulating enzyme concentration or activity |
Elevated circulating hepatic transaminase concentration |
Reduced uroporphyrinogen decarboxylase activity |
Diabetes mellitus |
Increased fecal porphyrin |
Elevated hepatic iron concentration |
Hepatic steatosis |
Increased urinary porphobilinogen |
Porphyrinuria |
Corneal scarring |
Scarring |
Disease(s) Associated with CYP1A2 | ||||||||||||||||
porphyria cutanea tarda |
Mouse Phenotypes | cyanosis |
decreased body temperature |
abnormal physiological response to xenobiotic |
decreased physiological sensitivity to xenobiotic |
decreased incidence of tumors by chemical induction |
abnormal xenobiotic pharmacokinetics |
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Availability | Mouse Genotype | ||||||
Cyp1a2tm1Dwn/Cyp1a2tm1Dwn | |||||||
Cyp1a2tm1Gonz/Cyp1a2tm1Gonz |
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 04/30/2024 MGI 6.23 |
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