Cyp1a2tm1Dwn
Targeted Allele Detail
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Symbol: |
Cyp1a2tm1Dwn |
Name: |
cytochrome P450, family 1, subfamily a, polypeptide 2; targeted mutation 1, Daniel W Nebert |
MGI ID: |
MGI:2182351 |
Synonyms: |
Cyp1a2-, HPRT KO BS-CL |
Gene: |
Cyp1a2 Location: Chr9:57584220-57590938 bp, - strand Genetic Position: Chr9, 31.3 cM
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Alliance: |
Cyp1a2tm1Dwn page
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Dioxin-induced hepatic injury in Cyp1a1tm1.1Dwn/Cyp1a1tm1.1Dwn and Cyp1a2tm1Dwn/Cyp1a2tm1Dwn mice
Show the 1 phenotype image(s) involving this allele.
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Germline Transmission: |
Earliest citation of germline transmission:
J:31730
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Parent Cell Line: |
E14TG2a (ES Cell)
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Strain of Origin: |
129P2/OlaHsd
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Allele Type: |
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Targeted (Null/knockout) |
Mutations: |
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Insertion, Intragenic deletion
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Mutation details: The insertion of an hprt gene, with the opposite orientation of the endogenous gene, deleted a portion of exon 2 and all of exons 3 through 5. This deleted region encoded the conserved cysteine-containing fragment and the cytochrome P450 tridecapeptide. Northern blot analysis of total hepatic RNA obtained from beta-naphthoflavone-treated animals showed a lack of transcript in homozygous mutant mice. Failure of homozygous mutant mice to metabolize zoxazolamine, a muscle relaxant, indicated a lack of functional protein.
(J:31730)
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View phenotypes and curated references for all genotypes (concatenated display).
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Original: |
J:31730 Liang HC, et al., Cyp1a2(-/-) null mutant mice develop normally but show deficient drug metabolism. Proc Natl Acad Sci U S A. 1996 Feb 20;93(4):1671-6 |
All: |
30 reference(s) |
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