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. 2021 Feb 11;12(2):263. doi: 10.3390/genes12020263

Table 1.

Summary of point mutations identified to date in LSDMCA.

Gene Gene OMIM# Nucleotide Change Type of Mutation Predicted Protein Disease Symbol Disease OMIM# Ref
HCCS 300056 c.589C>T Nonsense p.R197* a MLS/ 309801 [2,13,14]
c.649C>T Missense p.R217C MIDAS
c.475G>A Missense p.E159K MCOPS7
c.[=/524_525delAG] Frameshift p.[=/E175Vfs*30] LSDMCA1
COX7B 300885 c.196delC Frameshift p.L66Cfs*48 LSDMCA2 300887 [3]
c.41-2A>G Frameshift p.V14Gfs*19
c.55C>T Nonsense p.E19*
NDUFB11 300403 c.262C>T Nonsense p.Arg88* LSDMCA3 300952 [4]
c.402delG Frameshift p.Arg134Serfs*3

a This mutation was identified in two different patients (see also Table S1). Ref, references.