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The open reading frame was replaced with one containing two point mutations (TTC to CGC) in exon 8. These mutations result in an amino acid substitution of arginine for phenylalanine at position 1128 (F1128R). An upstream floxed neo was removed by germ line, cre mediated recombination. This mutation is expected to reduce Homer binding. (J:151084)
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
