This phenotypic mutant was the result of random integration of 8-10 copies of a tyrosinase expressing transgene. The insertion was accompanied by a 550 kb deletion that affects several genes in the region, including Rxfp2 (also known as Great). (J:69948)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
FVB/N
--
Insertion, Intergenic deletion
Recessive
--
--
9

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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