Description : Lyso-phosphatidylcholine acyltransferase; required for normal phospholipid content of mitochondrial membranes; major determinant of the final acyl chain composition of the mitochondrial-specific phospholipid cardiolipin; mutations in human ortholog tafazzin (TAZ) cause Barth syndrome, a rare X-linked disease characterized by skeletal and cardiomyopathy and bouts of cyclic neutropenia; a specific splice variant of human TAZ can complement yeast null mutant [Source:SGD;Acc:S000006344]
Gene families : OG_03_0002746 (OF) Phylogenetic Tree(s): OG0002746_tree
Note:Only the main profile, including all conditions, is shown. Additional statistics and tissue specific profiles are available here.
Type | Description | Actions |
---|---|---|
Neighborhood | HRR: YPR140W | |
Cluster | HCCA: Cluster_53 |
Type | GO Term | Name | Evidence | Source |
---|---|---|---|---|
MF | GO:0016746 | transferase activity, transferring acyl groups | IEA | Interproscan |
Type | GO Term | Name | Evidence | Source |
---|---|---|---|---|
No Predicted GO terms available for this sequence |
InterPro domains | Description | Start | Stop |
---|---|---|---|
IPR002123 | Plipid/glycerol_acylTrfase | 65 | 226 |
No external refs found! |