3-hydroxy-3-methylglutaryl-CoA synthase 2
| UniProt | Protein Name |
|---|---|
| A0A140VJL2 |
|
| P54868 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| kidney development |
|
|
| liver development |
|
|
| acetyl-CoA metabolic process |
|
|
| acetyl-CoA metabolic process |
|
|
| acetyl-CoA metabolic process |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrion |
|
|
| mitochondrion |
|
|
| mitochondrion |
|
|
| mitochondrion |
|
|
| mitochondrion |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| hydroxymethylglutaryl-CoA synthase activity |
|
|
| hydroxymethylglutaryl-CoA synthase activity |
|
|
| hydroxymethylglutaryl-CoA synthase activity |
|
|
| hydroxymethylglutaryl-CoA synthase activity |
|
|
| hydroxymethylglutaryl-CoA synthase activity |
|
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0081168 | HMG-CoA synthase 2 deficiency |
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0001250 | Seizure |
| HP:0001325 | Hypoglycemic coma |
| HP:0001939 | Abnormality of metabolism/homeostasis |
| HP:0001943 | Hypoglycemia |
| HP:0002013 | Vomiting |
| HP:0002014 | Diarrhea |
| HP:0002240 | Hepatomegaly |
| HP:0003593 | Infantile onset |
| Disease ID | Disease Name |
|---|---|
| OMIM:605911 |
|
| ORPHA:35701 |
|
| Species | Gene ID | Alliance of Genome Resources |
|---|---|---|
| 15360 | MGI:101939 |
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