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1 protein found in SwissVar (0 variants)

with gene/protein name Q6XZF7

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)
Q6XZF7 DNMBP_HUMAN an autosomal recessive ocular disease characterized by bilateral infantile or early-childhood-onset cataracts