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An A-to-G point mutation at coding nucleotide 518 in exon 5, resulting in an aspartic acid to glycine amino acid change at position 173 (p.D173G), was identified in the Cx3cr1tm1Litt line. Backcrossing with BALB/c mice segregated the two mutations. (J:215293)
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
