Symbol Name ID |
Fech
ferrochelatase MGI:95513 |
Darker colors indicate more annotations |
Human Phenotypes | Absent eyebrow |
Loss of eyelashes |
Erythema |
Jaundice |
Eczematoid dermatitis |
Alopecia |
Hypertrichosis |
Hyperpigmentation of the skin |
Hypopigmentation of the skin |
Cutaneous photosensitivity |
Atypical scarring of skin |
Thickened skin |
Scleroderma |
Pruritus |
Disease(s) Associated with FECH | ||||||||||||||
cutaneous porphyria | ||||||||||||||
erythropoietic protoporphyria |
Mouse Phenotypes | skin photosensitivity |
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Availability | Mouse Genotype | |
Fechm1Pas/Fechm1Pas | ||
Fechtm1Dab/Fech+ |
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 05/28/2024 MGI 6.13 |
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