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ENU-induced C to T transition at position 27320144 bp of the genomic sequence of Vldlr, affecting nucleotide 2239 of the mRNA in exon 15 (NCBI RefSeq: (NM_013703.2), Variant 1; NM_001161420.1, variant 2). The mutation results in coding of a premature stop codon after amino acid 746 (R747*). (J:176337)
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
