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EN
ENU-induced T-to-A mutation at base pair 66,696,520 (GRCm38) on chromosome 15, or base pair 25,767 in the GenBank genomic region NC_000081 encoding Tg. The mutation corresponds to residue 4,077 in the NM_009375 mRNA sequence in exon 19 of 48 total exons. The mutation results in an isoleucine to lysine substitution of position 1,352 (p.I1352K) in the encoded peptide. (J:265197)
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
