The gene was disrupted by replacement of exon 3 with a neomycin resistance cassette via homologous recombination. Absence of protein (both long and short forms) was confirmed by Western blot analysis of retinal extracts from homozygous mutant mice. Western blotting of mutant protein extracts also revealed loss of RGS6, RGS7, and RGS11 and a reduction of RGS9 (<5% of wild-type levels) in mutant retinas, as well as absence of RGS9 and RGS7 in mutant striatum, indicating instability of RGS proteins containing the G protein gamma-like (GGL) domain. (J:83620)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129S1/Sv-Oca2+ Tyr+ Kitl+
Targeted
Insertion, Intragenic deletion
--
1
2
19

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

References Literature

Title
PMID
Journal
Year
IF
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