This mutation was discovered among G3 progeny of an ENU mutagenized male mouse. It was mapped to Chromosome 13 between the centromere and D13Mit14, the region containing the Lyst locus. Sequence analysis of 90% of the Lyst gene from mutant mice has not discovered a mutation. However, in a complementation test this mutation was found to be allelic with beige Beutler (Lystbg-Btlr), in which a mutation in the Lyst gene has been identified.

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6J
Chemically induced
Undefined
Recessive
1
2
--

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:
Show/Hide columns
Phenotypes

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top