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1 protein found in SwissVar (0 variants)

with gene/protein name P11161

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)
P11161 EGR2_HUMAN neuropathy, congenital hypomyelinating, 1, autosomal recessive
P11161 EGR2_HUMAN charcot-marie-tooth disease 1d
P11161 EGR2_HUMAN dejerine-sottas syndrome