Symbol
Name
ID
|
|
|
Synonyms
|
VLCAD
|
|
Genetic Map
|
|
|
Sequence Map
|
|
Mammalian homology
|
|
|
Sequences
|
All sequences(22)
|
Alleles and phenotypes
|
All alleles(2) :
Targeted, knock-out(2)
| Homozygous mutant animals exhibit mild steatosis, lipid accumulation in myocytes, increased fatigue, impaired temperature regulation, increased susceptibility to arrhythmia, accumulation of long-chain acylcarnitines, and lower free carnitine levels. |
Associated Human Diseases (1)
Alleles Annotated to Human Diseases (2)
|
|
Polymorphisms
|
RFLP(1)
SNPs within 2kb(51 from dbSNP Build 128)
|
Gene Ontology (GO) classifications
|
|
|
Expression
|
Literature Summary: (2 records)
Data Summary:
Assays (2)
Results (28)
Tissues (21)
Theiler Stages: 10,18,23,25,28
| |
Assay Type |
Assays |
|
Results |
| |
Northern blot |
2 |
|
28 |
cDNA source data(268)
External Resources:
Allen Brain Atlas
GEO
ArrayExpress
|
Molecular reagents
|
All nucleic(274)
Genomic(4)
cDNA(268)
Primer pair(1)
Other(1)
Microarray probesets(2)
|
|
Pathways
|
|
Other database links
|
|
Protein domains
|
| 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
|
|
References
|
(Earliest)
J:42861
Aoyama T et al.,
"A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase."
Biochem Biophys Res Commun 1993 Mar 31;191(3):1369-72
(Latest)
J:154719
Cox KB et al.,
"Cardiac hypertrophy in mice with long-chain acyl-CoA dehydrogenase or very long-chain acyl-CoA dehydrogenase deficiency."
Lab Invest 2009 Dec;89(12):1348-54
|
All references(27)
|