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Mice carrying Tg(Hba1-Gfp)1Ew were treated with ENU. A T to C transition was identified at position 2249 in exon 19 causing a leucine-to-proline substitution at amino acid position 750. Immunofluorescence analysis detected protein expression in mutant MEFs. This is a hypomorphic allele. (J:99816, J:181888)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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References Literature
Title
PMID
Journal
Year
IF
