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This TALEN-mediated discontinuous deletion of 3 base pairs in exon 9, coding nucleotide 3481 and nucleotides 3483 and 3484, causes a substitution of glycine in place of arginine at amino acid 1161 and deletion of cysteine 1162. (J:265859)
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
