Symbol
Name
ID
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Synonyms
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D17825
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Genetic Map
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Sequence Map
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Mammalian homology
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Sequences
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All sequences(31)
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Alleles and phenotypes
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All alleles(1) :
Targeted, other(1)
| Homozygotes for a targeted null mutation exhibit a mild motor deficit associated with a diffuse spongiform myelinopathy and elevated levels of glutaric acid and 3-hydroxyglutaric acid. |
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Polymorphisms
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RFLP(1)
SNPs within 2kb(65 from dbSNP Build 128)
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Gene Ontology (GO) classifications
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Expression
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Literature Summary: (1 records)
Data Summary:
Assays (1)
Results (46)
Tissues (45)
Images (1)
Theiler Stages: 23,28
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Assay Type |
Assays |
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Results |
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RT-PCR |
1 |
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46 |
cDNA source data(77)
External Resources:
Allen Brain Atlas
GEO
ArrayExpress
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Molecular reagents
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All nucleic(83)
Genomic(5)
cDNA(77)
Primer pair(1)
Microarray probesets(2)
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Other database links
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Protein domains
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| InterPro ID |
Description |
| IPR006089 |
Acyl-CoA dehydrogenase, conserved site |
| IPR006090 |
Acyl-CoA oxidase/dehydrogenase, type 1 |
| IPR006091 |
Acyl-CoA oxidase/dehydrogenase, central domain |
| IPR006092 |
Acyl-CoA dehydrogenase, N-terminal |
| IPR009075 |
Acyl-CoA dehydrogenase/oxidase C-terminal |
| IPR009100 |
Acyl-CoA dehydrogenase/oxidase |
| IPR013764 |
Acyl-CoA oxidase/dehydrogenase, type1/2, C-terminal |
| IPR013786 |
Acyl-CoA dehydrogenase/oxidase, N-terminal |
Graphical View
of Protein Domain Structure
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References
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(Earliest)
J:28406
Koeller DM et al.,
"Cloning, structure, and chromosome localization of the mouse glutaryl-CoA dehydrogenase gene."
Genomics 1995 Aug 10;28(3):508-12
(Latest)
J:151002
Pagliarini DJ et al.,
"A mitochondrial protein compendium elucidates complex I disease biology."
Cell 2008 Jul 11;134(1):112-23
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All references(17)
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Other accession IDs
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MGD-MRK-25973, MGI:2142490, MGI:2142887
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