3-hydroxy-3-methylglutaryl-CoA reductase
| UniProt | Protein Name |
|---|---|
| P04035 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| cholesterol biosynthetic process |
|
|
| isoprenoid biosynthetic process |
|
|
| isoprenoid biosynthetic process |
|
|
| isoprenoid biosynthetic process |
|
|
| visual learning |
|
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| peroxisomal membrane |
|
|
| peroxisomal membrane |
|
|
| peroxisomal membrane |
|
|
| endoplasmic reticulum |
|
|
| endoplasmic reticulum membrane |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| hydroxymethylglutaryl-CoA reductase (NADPH) activity |
|
|
| hydroxymethylglutaryl-CoA reductase (NADPH) activity |
|
|
| hydroxymethylglutaryl-CoA reductase (NADPH) activity |
|
|
| hydroxymethylglutaryl-CoA reductase (NADPH) activity |
|
|
| protein binding |
|
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080000 | muscular disease | |
| DOID:14330 | Parkinson's disease | |
| DOID:10652 | Alzheimer's disease | |
| DOID:1094 | attention deficit hyperactivity disorder | |
| DOID:2841 | asthma | |
| DOID:3393 | coronary artery disease | |
| DOID:8805 | intermediate coronary syndrome | |
| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | |
| DOID:9351 | diabetes mellitus | |
| DOID:1307 | dementia |
| Species | Gene ID | Alliance of Genome Resources |
|---|---|---|
| 25675 | RGD:2803 | |
| 42803 | FB:FBgn0263782 | |
| 15357 | MGI:96159 | |
| 397750 | Xenbase:XB-GENE-5840728 | |
| 851171 | SGD:S000004442 | |
| 854900 | SGD:S000004540 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 6, 2026