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This ENU-induced mutation was isolated in a screen for abnormal behavior at the Mouse Mutagenesis Program Core Facility in Academia Sinica, Taiwan. A 7827-bp deletion spanning the promoter region, exon 1, and a part of intron1 in the Rab18 gene was identified. Western blot confirmed absence of protein in the cerebellum of homozygotes. (J:220974)
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
