alkylglycerone phosphate synthase
| GO Term | Evidence Code | PMID |
|---|---|---|
| lipid biosynthetic process |
|
|
| lipid biosynthetic process |
|
|
| lipid biosynthetic process |
|
|
| ether lipid biosynthetic process |
|
|
| ether lipid biosynthetic process |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrion |
|
|
| peroxisome |
|
|
| peroxisome |
|
|
| peroxisome |
|
|
| peroxisome |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| catalytic activity |
|
|
| protein binding |
|
|
| alkylglycerone-phosphate synthase activity |
|
|
| alkylglycerone-phosphate synthase activity |
|
|
| alkylglycerone-phosphate synthase activity |
|
| Gene Ontology |
|---|
| D-lactate dehydrogenase (cytochrome) activity |
| D-lactate dehydrogenase activity |
| FAD binding |
| catalytic activity |
| flavin adenine dinucleotide binding |
| lactate catabolic process |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110853 | rhizomelic chondrodysplasia punctata type 3 | |
| DOID:2580 | rhizomelic chondrodysplasia punctata |
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0001508 | Failure to thrive |
| HP:0003097 | Short femur |
| HP:0005792 | Short humerus |
| HP:0008873 | Disproportionate short-limb short stature |
| HP:0008905 | Rhizomelia |
| HP:0010655 | Epiphyseal stippling |
| Disease ID | Disease Name |
|---|---|
| OMIM:600121 |
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: April 6, 2026