SEPN1 Products

Description

The SEPN1 gene encodes a selenoprotein, which contains a selenocysteine (Sec) residue at its active site. The selenocysteine is encoded by the UGA codon that normally signals translation termination. The 3' UTR of selenoprotein genes have a common stem-loop st

Bioinformatics

Entrez	57190 Human
Uniprot	NP_996809 Human NP_065184 Human
Product By Gene ID	57190
Alternate Names	selN SelN rigid spine muscular dystrophy 1 selenoprotein N RSMD1 RSS SELNMDRS1 FLJ24021 selenoprotein N, 1

Diseases related to SEPN1

Discover more about diseases related to SEPN1.

Myopathy
Muscular Dystrophy
Dystrophy
Congenital Myopathy (disorder)
Weakness
Scoliosis, Unspecified
Congenital Muscular Dystrophy (disorder)
Central Core Myopathy (disorder)
Neuromuscular Diseases
Muscle Weakness
Congenital Structural Myopathy
Muscle Hypotonia
Congenital Fiber Type Disproportion
Malignant Hyperpyrexia Due To Anesthesia
Malignant Paraganglionic Neoplasm
Ophthalmoplegia
Respiratory Failure
Eichsfeld Type Congenital Muscular Dystrophy

Pathways for SEPN1

View related products by pathway and learn more about each of the pathways below.

Translation
Regeneration
Pathogenesis
Cell Death
Cell Proliferation
Selenocysteine Incorporation
Somitogenesis
Cytokine Secretion
Glycosylation
Muscle Contraction
Response To Caffeine
Localization
Muscle Atrophy
Spermatogenesis
Senescence
Swimming
Skeletal Muscle Contraction
Lymphocyte Proliferation
Secretion

PTMs for SEPN1

Learn more about PTMs related to SEPN1.

Phosphorylation
Glycosylation
Oxidation
Methylation

Bioinformatics Tool for SEPN1

Discover related pathways, diseases and genes to SEPN1. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.