|
Symbol Name ID |
Alas2
aminolevulinic acid synthase 2, erythroid MGI:87990 |
| Darker colors indicate more annotations |
| Human Phenotypes | Absent eyebrow |
Loss of eyelashes |
Erythema |
Jaundice |
Prolonged neonatal jaundice |
Eczematoid dermatitis |
Alopecia |
Hypertrichosis |
Hyperpigmentation of the skin |
Hypopigmentation of the skin |
Cutaneous photosensitivity |
Atypical scarring of skin |
Anemic pallor |
Thickened skin |
Scleroderma |
Pruritus |
| Disease(s) Associated with ALAS2 | ||||||||||||||||
| cutaneous porphyria | ||||||||||||||||
| erythropoietic protoporphyria | ||||||||||||||||
| hemochromatosis | ||||||||||||||||
| sideroblastic anemia 1 |
| Mouse Phenotypes | pallor |
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| Availability | Mouse Genotype | |
| Alas2tm1Mym/Y | ||
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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