Primary information |
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Humcfs Id | Humcfs_649 |
chromosome_number | chromosome1 |
name | FRA1L |
chrlocation | 61300001-84900000 |
cytoband | 1p31 |
type | Aphidicolin |
frequency | Common |
gene_ensembl_id | ENSG00000117054 |
gene_name | ACADM |
havana_transcript_id | OTTHUMT00000026967 |
gene_location | 75724351-75763679 |
gene_orientation | + |
exon_id | ENSE00001844831, ENSE00003661831, ENSE00003600551, ENSE00003643069, ENSE00003619848, ENSE00003667756, ENSE00003640977, ENSE00003604105, ENSE00003533043, ENSE00003495277, ENSE00003668352, ENSE000015139 |
exon_number | 12 |
gene_description | acyl-CoA dehydrogenase, C-4 to C-12 straight chain |
disease_description | Deficiency 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_location | NA |
miRNA_strand | NA |
miRNA_id | NA |
miRNA_name | NA |
miRNA_derived | NA |
Technique | Karyotyping |
PMID | 20198338 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |