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- Table of Contents
Facts about Long-chain-fatty-acid--CoA ligase 4.
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Human | |
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Gene Name: | ACSL4 |
Uniprot: | O60488 |
Entrez: | 2182 |
Belongs to: |
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ATP-dependent AMP-binding enzyme family |
ACS4mental retardation, X-linked 68; acyl-CoA synthetase 4; acyl-CoA synthetase long-chain family member 4; EC 6.2.1.3; FACL4long-chain 4; LACS 4; LACS4MRX68; lignoceroyl-CoA synthase; Long-chain acyl-CoA synthetase 4; long-chain fatty-acid-Coenzyme A ligase 4; long-chain-fatty-acid--CoA ligase 4; mental retardation, X-linked 63; MRX63
Mass (kDA):
79.188 kDA
Human | |
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Location: | Xq23 |
Sequence: | X; NC_000023.11 (109641335..109733392, complement) |
Mitochondrion outer membrane; Single-pass type III membrane protein. Peroxisome membrane; Single-pass type III membrane protein. Microsome membrane; Single-pass type III membrane protein. Endoplasmic reticulum membrane; Single-pass type III membrane protein. Cell membrane.
PMID: 9598324 by Cao Y., et al. Cloning, expression, and chromosomal localization of human long-chain fatty acid-CoA ligase 4 (FACL4).
PMID: 9480748 by Piccini M., et al. FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation.