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FLASH GENE
Symbol ACADL contributors: - updated : 05-10-2006
HGNC name acyl-Coenzyme A dehydrogenase, long chain
HGNC id 88
Corresponding disease
ACADL acyl-CoA dehydrogenase, long chain, deficiency
Location 2q34      Physical location : 211.052.717 - 211.090.215
Synonym symbol(s) LCAD, ACAD4
EC.number 1.3.99.3, 1.3.99.13
DNA
TYPE functioning gene
STRUCTURE 37.00 kb     11 Exon(s)
10 Kb 5' upstream gene genomic sequence study
MAPPING cloned Y linked   status confirmed
RNA
TRANSCRIPTS type messenger
EXPRESSION
Type widely
constitutive of
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Digestiveliver    
tissue
SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
Blood / Hematopoietic    
Connective    
cells
SystemCellPubmedSpeciesStageRna symbol
Blood/Hematopoieticleukocyte
cell lineage
cell lines
fluid/secretion
at STAGE
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
mono polymer homomer , tetramer
isoforms Precursor
HOMOLOGY
Homologene
FAMILY
CATEGORY enzyme
SUBCELLULAR LOCALIZATION     intracellular
intracellular,cytoplasm,organelle,mitochondria,matrix
basic FUNCTION
  • acyl-CoA dehydrogenase, long chain (C10-C18), unsaturated fatty acids, first step in the beta oxidation process
    • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism energetic , lipid/lipoprotein
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule cofactor, nucleotide,
    FAD+
    protein
    cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) ACADL
    related resource MITOP database
    Susceptibility susceptibility to autism
    Variant & Polymorphism
    Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS
    ACADL deficiency increasing death rate in imbryo at the morula to blastocyst conversion