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1 protein found in SwissVar (0 variants)

with gene/protein name O00142

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)
O00142 KITM_HUMAN mitochondrial dna depletion syndrome 2
O00142 KITM_HUMAN progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 3