Pou2f1tm1Shrp
Targeted Allele Detail
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Symbol: |
Pou2f1tm1Shrp |
Name: |
POU domain, class 2, transcription factor 1; targeted mutation 1, Phillip A Sharp |
MGI ID: |
MGI:3028868 |
Synonyms: |
Oct-1- |
Gene: |
Pou2f1 Location: Chr1:165692723-165830247 bp, - strand Genetic Position: Chr1, 73.21 cM
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Alliance: |
Pou2f1tm1Shrp page
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Germline Transmission: |
Earliest citation of germline transmission:
J:87664
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Parent Cell Line: |
J1 (ES Cell)
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Strain of Origin: |
129S4/SvJae
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Allele Type: |
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Targeted (Hypomorph) |
Mutations: |
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Insertion, Intragenic deletion
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Mutation details: Exon 3 was replaced with a floxed neo cassette. The deleted exon is common to all three known isoforms and does not overlap with Cd247, a locus that overlaps a distal portion of the Pou2f1 locus. Mutant transcript, in which exon 2 aberrantly splices to exon 4a, was identified by RT-PCR analysis of homozygous mutant MEFs. The aberrant splicing results in a frameshift mutation which consequently generates a nonsense mutation and precludes the translation of two-thirds of the mature protein including the DNA-binding domain. Supershift analysis of DNA binding assays using nuclear extracts from homozygous cells detected very low levels of protien, thus this is a severely hypomorphic allele.
(J:87664)
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View phenotypes and curated references for all genotypes (concatenated display).
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Original: |
J:87664 Wang VE, et al., Embryonic lethality, decreased erythropoiesis, and defective octamer-dependent promoter activation in Oct-1-deficient mice. Mol Cell Biol. 2004 Feb;24(3):1022-32 |
All: |
7 reference(s) |
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