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This mutation, discovered by its phenotype among progeny of an ENU mutagenized male mouse, has been identified as a T to C transition in the donor splice site of intron 6, at position 113891 of the gene (Genbank genomic region NC_000067 for linear genomic DNA sequence of Epha4). (J:156850)
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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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
