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EN
ENU mutagenesis induced a single nucleotide mutation to C of the first T (shown here in lower case)(96129096 bp on Chr9; NCBI v38) in G-GtAATGGTT (hyphen depicts exon-intron boundary). This mutation affects the exon 2-3 splice donor site. (J:243852)
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
