| Gene: | | ACLY ( Homo sapiens ) | | ATP citrate lyase |
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| Description: | ATP citrate lyase is the primary enzyme responsible for the synthesis of cytosolic acetyl-CoA in many tissues. The enzyme is a tetramer (relative molecular weight approximately 440,000) of apparently identical subunits. It catalyzes the formation of acetyl-CoA and oxaloacetate from citrate and CoA with a concomitant hydrolysis of ATP to ADP and phosphate. The product, acetyl-CoA, serves several important biosynthetic pathways, including lipogenesis and cholesterogenesis. In nervous tissue, ATP citrate-lyase may be involved in the biosynthesis of acetylcholine. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq] |
| Synonyms: | ATPCL; ACL; CLATP; |
| Gene Type: | protein-coding |
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| Additional Data |
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| Homologs |
| Mus musculus: Acly See the Mouse gene in context in: UCSC NCBI MapViewer |
| Rattus norvegicus: Acly See the Rat gene in context in: UCSC NCBI MapViewer |
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| Rattus norvegicus | Acly | genome assembly 3.1 | 10 | 89435312 - 89485719 | | | | Rat Celera Assembly | 10 | 84129406 - 84179897 | | | | RGSC genome assembly v3.4 | 10 | 89420941 - 89471349 | | | | Cytogenetic | 10 | q32.1 | | Mus musculus | Acly | Mouse genome assembly build 36.1 | 11 | 100337670 - 100389215 | | | | Cytogenetic | 11 | 11 D | | Homo sapiens | ACLY | human genome assembly | 17 | 37276706 - 37328798 | | | | Human genome assembly build 36.2 | 17 | 37276705 - 37328798 | | | | Cytogenetic | 17 | q12-q21 | | | | View comparative maps: | NCBI MapViewer | |
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Annotation |
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External Links |
| Databases | | DATABASE | ID | SOURCE | | OMIM: | 108728 | ENTREZGENE | | HGNC ID: | ACLY | ENTREZGENE | | Entrez Gene: | ACLY | ENTREZGENE | | KEGG Report: | hsa:47 | ENTREZGENE | | HomoloGene Group ID: | 854 | ENTREZGENE | | HPRD ID: | 00155 | ENTREZGENE | | KEGG Pathway: | 00720 | ENTREZGENE | | KEGG Pathway: | 00020 | ENTREZGENE |
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Database Information |
| RGD ID | 10065 |
| History | No Nomenclature events are recorded for this object |