ALDH3A2 wt Allele

Preferred Label : ALDH3A2 wt Allele;

NCIt synonyms : ALDH10; Aldehyde Dehydrogenase 3 Family, Member A2 Gene; FALDH; Aldehyde Dehydrogenase 3 Family Member A2 wt Allele; SLS; Aldehyde Dehydrogenase, Family 3, Subfamily A, Member 2 Gene;

NCIt definition : Human ALDH3A2 wild-type allele is located in the vicinity of 17p11.2 and is approximately 38 kb in length. This allele, which encodes aldehyde dehydrogenase family 3 member A2 protein, is involved in the conversion of aldehydes to fatty acids. Mutations in the gene are associated with Sjogren-Larsson syndrome.;

NCI Metathesaurus CUI : CL1927182;

GenBank Accession Number : L47162;

Details

Origin ID

C205134;

OMIM relation
- Aldehyde dehydrogenase, family 3, subfamily a, member 2 [OMIM gene]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 17p11.2 [NCIt concept]
gene_is_element_in_pathway
- Arginine and Proline Metabolism Pathway [NCIt concept]
- Ascorbate and Aldarate Metabolism Pathway [NCIt concept]
- Beta-Alanine Metabolism Pathway [NCIt concept]
- Fatty Acid Metabolism Pathway [NCIt concept]
- Glycerolipid Metabolism Pathway [NCIt concept]
- Glycolysis/Gluconeogenesis Pathway [NCIt concept]
- Histidine Metabolism Pathway [NCIt concept]
- Lysine Degradation Pathway [NCIt concept]
- Pantothenate and CoA Biosynthesis Pathway [NCIt concept]
- Pyruvate Metabolism 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]
- Histogenic Process [NCIt concept]
- Nervous System Development [NCIt concept]
- Oxidation [NCIt concept]
- Oxidation/Reduction [NCIt concept]

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