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A C-to-T transition mutation at nucleotide 854 is predicted to result in a proline to leucine substitution at residue 285 (P285L in TMV region). Neither of the flanking markers D14Mit38 and D14Mit42 (2 cM apart) was deleted in this mutation. (J:16291, J:44601)
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
