3-hydroxy-3-methylglutaryl-CoA reductase

Summary
Gene Symbol
  • HMGCR
Organism
Homo sapiens (human)
NCBI Gene
3156
PubChem
3156
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Cholesterol biosynthesis
  • Disease variant
  • Endoplasmic reticulum
  • Glycoprotein
  • Isopeptide bond
  • Limb-girdle muscular dystrophy
  • NADP
  • Oxidoreductase
  • Peroxisome
  • Phosphoprotein
  • Reference proteome
  • Transmembrane helix
  • Ubl conjugation
Proteins
Displaying 1 entry
UniProt Protein Name
P04035
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
Disease
Disease Ontology
Displaying entries 1 - 10 of 11 in total
DO ID Disease Name Source
DOID:0080000 muscular disease
DOID:0110274 autosomal recessive limb-girdle muscular dystrophy
DOID:10652 Alzheimer's disease
DOID:1094 attention deficit hyperactivity disorder
DOID:1307 dementia
DOID:14330 Parkinson's disease
DOID:2841 asthma
DOID:3393 coronary artery disease
DOID:8805 intermediate coronary syndrome
DOID:9351 diabetes mellitus

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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