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This spontaneous thymine to cytosine point substitution in the ATG start codon of exon 1a has exon 3 as the next in-frame start codon so is predicted to cause a start-loss variant disrupting the first zinc finger domain. Expression of the Rorb1 transcript in brain and retina is significantly increased and the Rorb2 transcript significantly decreased in retina. (J:337403)
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
