| ALDOA |
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| Identifiers |
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| Aliases | ALDOA, ALDA, GSD12, HEL-S-87p, aldolase, fructose-bisphosphate A, Aldolase A |
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| External IDs | OMIM: 103850; MGI: 87994; HomoloGene: 141054; GeneCards: ALDOA; OMA:ALDOA - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 7 (mouse) |
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| | Band | 7|7 F3 | Start | 126,394,406 bp |
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| End | 126,399,923 bp |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - gastrocnemius muscle
- muscle of thigh
- skeletal muscle tissue
- superior frontal gyrus
- apex of heart
- prefrontal cortex
- right frontal lobe
- primary visual cortex
- left ventricle
- right auricle of heart
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| | Top expressed in | - medial head of gastrocnemius muscle
- ankle
- vastus lateralis muscle
- triceps brachii muscle
- sternocleidomastoid muscle
- temporal muscle
- digastric muscle
- masseter muscle
- tibialis anterior muscle
- knee joint
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| | More reference expression data |
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| BioGPS | |
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| Wikidata |
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Aldolase A (ALDOA, or ALDA), also known as fructose-bisphosphate aldolase, is an enzyme that in humans is encoded by the ALDOA gene on chromosome 16.
The protein encoded by this gene is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate (G3P) and dihydroxyacetone phosphate (DHAP). Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing and alternative promoter usage results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 3 and 10.