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1 protein found in SwissVar (0 variants)

with gene/protein name O75787

Disclaimer: The query results are intended for research purposes only, not for clinical and diagnostic use.

Accession Entry name Disease Variants 3D mapping
(variant position)
O75787 RENR_HUMAN mental retardation, x-linked, with epilepsy
O75787 RENR_HUMAN parkinsonism with spasticity, x-linked
O75787 RENR_HUMAN glycosylation disorder with autophagic defects characterized by serum protein hypoglycosylation, immunodeficiency, liver disease, psychomotor impairment, and cutis laxa