HADH wt Allele

Preferred Label : HADH wt Allele;

NCIt synonyms : HADHSC; L-3-Hydroxyacyl-Coenzyme A Dehydrogenase, Short Chain Gene; HHF4; MSCHAD; HADH1; SCHAD; HCDH; Hydroxyacyl-CoA Dehydrogenase wt Allele; HAD;

NCIt definition : Human HADH wild-type allele is located in the vicinity of 4q25 and is approximately 46 kb in length. This allele, which encodes hydroxyacyl-coenzyme A dehydrogenase, mitochondrial protein, is involved in the regulation of insulin secretion and the oxidation of short- and medium-chain fatty acids. Mutation of the gene is associated with both 3-hydroxyacyl-CoA dehydrogenase deficiency and familial hyperinsulinemic hypoglycemia 4.;

GenBank Accession Number : X96752;

Details

Origin ID

C201708;

OMIM relation
- 3-hydroxyacyl-coa dehydrogenase [OMIM gene]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 4q25 [NCIt concept]
gene_is_element_in_pathway
- Butanoate Metabolism Pathway [NCIt concept]
- FOXA2 and FOXA3 Transcription Factor Signaling Pathway [NCIt concept]
- Fatty Acid Biosynthesis Pathway [NCIt concept]
- Fatty Acid Elongation Pathway in Mitochondria [NCIt concept]
- Fatty Acid Metabolism Pathway [NCIt concept]
- Lysine Degradation Pathway [NCIt concept]
- Tryptophan Metabolism Pathway [NCIt concept]
- Valine, Leucine and Isoleucine Degradation Pathway [NCIt concept]
gene_plays_role_in_process
- Catabolic Process [NCIt concept]
- Fatty Acid Metabolism [NCIt concept]
- Oxidation [NCIt concept]
- Oxidation/Reduction [NCIt concept]

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