|
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 04/16/2024 MGI 6.23 |
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