This allele is defined by a noncomplementation test with C57BL/6JHamSlc-Lystbg. This mutation is the result of a 4 bp deletion in Lyst exon 29 that produced frameshift mutations resulting in 3 amino-acid substitutions and creation of 6 new stop codons. The sequence data was deposited in DDBJ under Accession number LC508235. (J:281218)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6JJcl
Spontaneous
Intragenic deletion
--
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:
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Phenotypes

References Literature

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PMID
Journal
Year
IF
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