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Allele : Fech<m1Pas> ferrochelatase; ferrochelatase deficiency, mutation 1, Institut Pasteur

Primary Identifier	MGI:1858114	Allele Type	Chemically induced (ENU)
Gene	Fech	Inheritance Mode	Recessive
Strain of Origin	129/Sv x BALB/c	Is Recombinase	false
Is Wild Type	false

molecularNote

This mutation is a T-to-A transversion at position 293, resulting in a methionine to lysine substitution at position 98 of the encoded protein.

mutations:
Single point mutation

synonyms:
fch,
fch

earliestPublication:
Tutois S, et al. (1991) Erythropoietic protoporphyria in the house mouse. A recessive inherited ferrochelatase deficiency with anemia, photosensitivity, and liver disease. J Clin Invest 88(5):1730-6

1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

Other

2 Carried By

0 Driven By

22 Publication categories

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