Ercc8tm1Jhjh
Targeted Allele Detail
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Symbol: |
Ercc8tm1Jhjh |
Name: |
excision repaiross-complementing rodent repair deficiency, complementation group 8; targeted mutation 1, Jan H J Hoeijmakers |
MGI ID: |
MGI:2449180 |
Synonyms: |
Csa- |
Gene: |
Ercc8 Location: Chr13:108295265-108331898 bp, + strand Genetic Position: Chr13, 59.69 cM, cytoband D
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Alliance: |
Ercc8tm1Jhjh page
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Microglia activation in the white matter in Ercc2, Ercc6, and Ercc8 mutants
Show the 1 phenotype image(s) involving this allele.
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Germline Transmission: |
Earliest citation of germline transmission:
J:74959
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Parent Cell Line: |
E14 (ES Cell)
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Strain of Origin: |
129P2/OlaHsd
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Allele Type: |
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Targeted (Null/knockout) |
Mutation: |
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Insertion
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Mutation details: The gene was disrupted by insertion of a PGK-hygro cassette into exon 2 (at amino acid 42) via homologous recombination. Absence of gene expression was verified by Western blot analysis of homozygous mutant MEFs using an antibody directed against the C-terminal domain of the human protein.
(J:74959)
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View phenotypes and curated references for all genotypes (concatenated display).
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Mouse strains and cell lines
available from the International Mouse Strain Resource
(IMSR) |
Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available
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Carrying any Ercc8 Mutation: |
31 strains or lines available
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Original: |
J:74959 van der Horst GT, et al., UVB radiation-induced cancer predisposition in Cockayne syndrome group A (Csa) mutant mice. DNA Repair (Amst). 2002;1:143-57 |
All: |
9 reference(s) |
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