LYAG

Lysosomal alpha-glucosidase

Essential for the degradation of glycogen in lysosomes (PubMed:14695532, PubMed:18429042, PubMed:1856189, PubMed:7717400). Has highest activity on alpha-1,4-linked glycosidic linkages, but can also hydrolyze alpha-1,6-linked glucans (PubMed:29061980).

Associated with:

Acute Kidney Injury
Alanine Transaminase
Albumin
Alcohol Dependence
Alkaline Phosphatase
Anxiety
Aspartate Transaminase
B Cell Disorders
Basophils
Bilirubin
BMI
Breast Cancer
C Reactive Protein
Calcium
Calcium Albumin Ratio
Cancer
Creatinine
Depression
Diastolic Blood Pressure
Eosinophils
Erythrocyte Sedimentation Rate
Estimated Glomerular Filtration Rate
Fibromyalgia
Folate
FT3 FT4 Ratio
Gallstones
Gamma Glutamyltransferase
Glucose
Granulocytes
HbA1c
Heartrate
Hematocrit
Hemoglobin
High Density Lipoprotein Cholesterol
Hypertension
IgA
Lactate Dehydrogenase
Liver Cirrhosis
Low Density Lipoprotein Cholesterol
Lymphocytes
Lymphoproliferative Diseases
Metabolic Syndrome
Monocytes
Myeloproliferative Neoplasm
Neuropathic Pain
Neutrophils
Panic Disorder
Persistent Mood Affective Disorders
Phobias
Plasma Prothrombin Time
Platelet
Primary Biliary Cirrhosis
Red Blood Cell Count
Severe Obesity (BMI > 35)
Sleep Disorders
Systemic Lupus
Systolic Blood Pressure
Testosterone
Thyroid FT3
Thyroid FT4
Total Cholesterol
Transferrin Saturation
Triglyceride
Type 2 Diabetes
Urea
Uric Acid
Urine Protein
Vitamin D
Weight
White Blood Cell
Hypoxia
Myogenesis

Matrix Type

Tissue/Cells

Gene Symbol

UniProt ID

P10253

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LYAG

Lysosomal alpha-glucosidase

Associated with:

Matrix Type

Gene Symbol

UniProt ID

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