The C57BL/6ByJ sequence was identical to that of C57BL/6 (NR_038116). Both strains have genomic sequences that contains a G to A substitution and single cytosine nucleotide deletion at positions 99 and 102, respectively, of the Balb/c reference sequence (Fig. 2d). The single base pair deletion is predicted to result in a frameshift mutation and production of a truncated version of the protein. (J:319051)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
C57BL/6ByJ
Spontaneous
Intragenic deletion, Single point
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--
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2

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

References Literature

Title
PMID
Journal
Year
IF
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