Emerin Products

Description

Emerin is a serine-rich nuclear membrane protein and a member of the nuclear lamina-associated protein family. It mediates membrane anchorage to the cytoskeleton. Dreifuss-Emery muscular dystrophy is an X-linked inherited degenerative myopathy resulting from mutation in the emerin gene.

Bioinformatics

Entrez	2010 Human
Uniprot	AAH00738 Human NM_000117 Human NP_000108 Human NP_000108.1 Human P50402 Human
Product By Gene ID	2010
Alternate Names	emerin Emery-Dreifuss muscular dystrophy LEM domain containing 5 STAEDMDLEMD5

Diseases related to Emerin

Discover more about diseases related to Emerin.

Alveolar Bone Loss
Gingival Recession
Periodontal Attachment Loss
Periodontal Pocket
Periodontitis
Neoplasms
Cardiac Arrest
Hemorrhage
Chronic Periodontitis
Dental Plaque
Malignant Neoplasms
Pain
Electromechanical Dissociation
Cardiac Fibrillation
Cardiac Arrhythmia
Heart Failure
Ventricular Fibrillation
Periodontal Diseases
Tissue Adhesions
Muscle Twitch

Pathways for Emerin

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Regeneration
Tissue Regeneration
Wound Healing
Cell Proliferation
Transport
Secretion
Sensitization
Angiogenesis
Cell Growth
Localization
Cell Differentiation
Cell Adhesion
Reflex
Muscle Contraction
Cell Cycle
Pathogenesis
Cell Migration
Osteoblast Differentiation
Inflammatory Response
Dehiscence

PTMs for Emerin

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Phosphorylation
Cleavage
Reduction
Oxidation
Demethylation
Hydroxylation
Deiodination
Dephosphorylation
Nitration
Glycosylation
Bromination

Bioinformatics Tool for Emerin

Discover related pathways, diseases and genes to Emerin. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.