Symbol Name ID |
Acbd5
acyl-Coenzyme A binding domain containing 5 MGI:1921409 |
Darker colors indicate more annotations |
Human Phenotypes | Very long chain fatty acid accumulation |
Disease(s) Associated with ACBD5 | |
retinal dystrophy with leukodystrophy |
Mouse Phenotypes | increased circulating creatinine level |
increased blood urea nitrogen level |
decreased circulating triglyceride level |
decreased circulating calcium level |
increased circulating alkaline phosphatase level |
decreased circulating serum albumin level |
decreased circulating total protein level |
improved glucose tolerance |
abnormal lipid homeostasis |
increased fatty acids level |
abnormal glycerol level |
abnormal ether lipid level |
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Availability | Mouse Genotype | ||||||||||||
Acbd5tm1a(EUCOMM)Wtsi/Acbd5tm1a(EUCOMM)Wtsi | |||||||||||||
Acbd5tm1b(EUCOMM)Wtsi/Acbd5tm1b(EUCOMM)Wtsi |
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 |
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