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Most of intron 10 and all of exon 11, encoding the linker domain and 5' terminus of the POUh domain, were replaced with a neo cassette via homologous recombination. RT-PCR detected the presence of a mutant transcript with exon 10 spliced to exon 12. EMSA analysis with nuclear extracts from spleen and thymus cells from heterozygous mice indicates that any truncated protein made is not able to bind DNA. This suggests that this mutation results in a null allele. (J:165572)
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
