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Phenotypes Associated with This Genotype
Genotype
MGI:6194786
Allelic
Composition
Abcd1tm1Kan/Y
Gt(ROSA)26Sortm2.1(CAG-ELOVL1)Geno/Gt(ROSA)26Sor+
Cnptm1(cre)Kan/Cnp+
Genetic
Background
involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Abcd1tm1Kan mutation (1 available); any Abcd1 mutation (11 available)
Cnptm1(cre)Kan mutation (0 available); any Cnp mutation (18 available)
Gt(ROSA)26Sortm2.1(CAG-ELOVL1)Geno mutation (0 available); any Gt(ROSA)26Sor mutation (510 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• mice exhibit very-long-chain fatty acid accumulation in different lipid classes and acylcarnitines
• C26:0 levels are increased 15-fold in brain and 12-fold in spinal cord
• 1-hexacosanoyl-sn-glycero-3-phosophocholine (C26:0-lysoPC) levels are increased 13-fold in the brain, 24-fold in the spinal cord, and 17-fold in the blood
• C26:0-carnitine levels are increased 40-fold in brain, 33-fold in spinal cord, and 16-fold in the blood

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
adrenoleukodystrophy DOID:10588 OMIM:300100
J:257393


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
01/14/2020
MGI 6.14
The Jackson Laboratory