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EN
ENU mutagenesis induced a single nucleotide deletion of a C at 96140630 or 96140631 bp (NCBI v38) on chromosome 9 at position 607 or 608 bp within transcript Ensembl ENSMUST00000085217. This mutation causes a frameshift and subsequent coding of one unrelated amino acid (p.Thr174Pro) followed by a premature stop (p.Leu175Stop) in the 516 (variant 1) or 534 (variant 2) amino acid peptide. (J:243852)
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
