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EN
ENU-induced T to A transversion at base pair 20,451,862 (v38) on chromosome 18, or base pair 15,688 in the GenBank genomic region NC_000084 for the gene. The mutation corresponds to residue 766 in the NM_181564 mRNA sequence in exon 6 of 16 total exons. The mutation results in a valine (V) to glutamic acid (E) substitution at position 211 (V211E) in the protein. (J:255183)
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
