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The C variant of SNP rs46447118 is detected in, amongst others, 129P2/OlaHsd, 129S1/SvImJ, 129S5SvEvBrd, A/J, BALB/cJ ,C57BL/6NJ, LG/J and SM/J. (J:211326)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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
