Apolipoprotein H

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Apolipoprotein H
[[Image:{{{Image}}}|thumb|220px|2D structure for Apolipoprotein H]]
Chemical Name
Chemical Formula
CAS Number
Chemical Information
Biochemical Taxonomy
Functional Taxonomy
Nutritional Taxonomy
Metabolic Pathways
Biofluid Location
Tissue Location
Normal Biofluid Concentrations
Normal Tissue Concentrations
Diseases / Conditions Related to Nutrition
Other (Monogenic Disorders)
Abnormal Biofluid Concentrations
Abnormal Tissue Concentrations
Physiological Processes
Authors: L. Pellis
Affiliations: TNO, the Netherlands


Contents

Introduction

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The human Apolipoprotein H (ApoH) molecule, also known as beta 2 glycoprotein 1, is expressed by placental trophoblast cells at high levels. Although the normal physiological role is not known, the protein appears to act as a co-factor for the binding of autoantibodies to phospholipids in trophoblasts, which is a process involved in the pathogenesis of recurrent miscarriage (antiphospholipid syndrome).

Biological Function

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Apolipoprotein H is an essential cofactor for the binding of certain antiphospholipid antibodies to anionic phospholipid.

Catabolism

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Diseases / Conditions Related to Nutrition

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Associated decreased protein/metabolite profile

Associated increased protein/metabolite profile

Other (Monogenic) Disorders

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Nutritional Information

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Drivers for biological variation

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Vulnerable groups

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Other resources

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Links

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OMIM

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