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Slc27a2tm1Kds
Targeted Allele Detail
Summary
Symbol: Slc27a2tm1Kds
Name: solute carrier family 27 (fatty acid transporter), member 2; targeted mutation 1, Kirby D Smith
MGI ID: MGI:2663647
Gene: Slc27a2  Location: Chr2:126394944-126430163 bp, + strand  Genetic Position: Chr2, 61.76 cM
Alliance: Slc27a2tm1Kds page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:83438
Parent Cell Line:  J1 (ES Cell)
Strain of Origin:  129S4/SvJae
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsThe 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)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Slc27a2 Mutation:  36 strains or lines available
References
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
All:  6 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory