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The Szt1 mutation represents a genomic deletion of about 300 kb of mouse chromosome 2. The deletion involves 3 known genes including those encoding the potassium channel, Kcnq2, and the nicotinic acetylcholine receptor subunit, Chrna4, and ADP-ribosylation factor GTPase activating protein 1, Arfgap1. (J:82964)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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
