NOC4L

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Description

The NOC4L (nucleolar complex associated 4 homolog) is a protein-coding gene located on chromosome 12.

NOC4L is also known as NET49, NOC4, UTP19.

Associated Diseases

• Parkinson disease
• multiple sclerosis
• lysosomal storage disease
• Alzheimer disease
• isolated asymptomatic elevation of creatine phosphokinase
• plasma fibronectin deficiency
• pentosuria
• myopathy due to calsequestrin and SERCA1 protein overload
• metabolic myopathy due to lactate transporter defect