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EN
This is a spontaneous 2 base pair insertion, CC, between Chromosome 2 position 155,944,953 bp, and 155,944,952 bp in exon 1 (GRCm38) changing the sequence from GAACCCCAGG to GAACCCCCCAGG, which is predicted to alter the amino acid sequence beginning at amino acid 37.
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
