Log In|Sign Up
EN
This spontaneous mutation (TT deletion in exon 57, c.7670_7671del, GRCm39:chr16:g.15587786_15587787del) was found in an inbred B10.S-H2s/SgSlc colony. The mutation causes a frameshift and premature stop codon (p.F2557Sfs*3). (J:341230)
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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
