Detailed description page of humcfs

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ACADM details
Primary information
gene_nameACADM
Humcfs IdHumcfs_649
chromosome_numberchromosome1
nameFRA1L
chrlocation61300001-84900000
cytoband1p31
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000117054
havana_transcript_idOTTHUMT00000026967
gene_location75724351-75763679
gene_orientation+
exon_idENSE00001844831, ENSE00003661831, ENSE00003600551, ENSE00003643069, ENSE00003619848, ENSE00003667756, ENSE00003640977, ENSE00003604105, ENSE00003533043, ENSE00003495277, ENSE00003668352, ENSE000015139
exon_number12
gene_descriptionacyl-CoA dehydrogenase, C-4 to C-12 straight chain
disease_descriptionDeficiency of butyryl-CoA dehydrogenase,Sudden infant death syndrome,Liver Failure,Non-alcoholic Fatty Liver Disease,Spots on skin,Liver Failure, Acute,Hypoglycemia,Lipid Metabolism Disorders,Lipid Metabolism, Inborn Errors,Necrotizing Enterocolitis,Medium-chain acyl-coenzyme A dehydrogenase deficiency,Idiopathic erosive/hemorrhagic gastritis,Vomiting,Acute gastric mucosal erosion,Exanthema,Myopathy,Obesity,Sudden death,Weight Gain
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID20198338
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