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| Nomenclature |
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Symbol:
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Slc27a2tm1Kds
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Name:
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solute carrier family 27 (fatty acid transporter), member 2;
targeted mutation 1, Kirby D Smith
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MGI ID: |
MGI:2663647 |
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Gene:
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Slc27a2
Location:
Chr2:126552407-126588243 bp, + strand
Genetic Position: Chr2,
61.76 cM
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:83438
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Parent Cell Line:
| J1 (ES Cell) |
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Strain of Origin:
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129S4/SvJae
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Mutation
description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutations: | |
Insertion, Intragenic deletion |
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Mutation details: The endogenous locus was disrupted by the insertion of neo selection cassette into exon 3, deleting 69 bp of this exon. Protein was undetected in homozygous mutant mice by Western blot analysis of liver, kidney, brain, and adrenal gland homogenates. (J:83438)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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| References |
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Original: |
J:83438
Heinzer AK et al.,
"A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy."
Hum Mol Genet 2003 May 15;12(10):1145-54
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All: |
2 reference(s)
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Analysis Tools
