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Identified in an ENU screen and mapped to Chromosome 15 0-73 (4 Mb). The mutation is an A-to-G coding change in the eleventh exon of the Grhl2 locus (c.A1451G; p.D484G, genomic position chr15:37,336,311 GRCm38) (J:174027)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
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
