CYC3/YAL039C Literature Guide Help

Other names published for CYC3: cytochrome c heme lyase, CCHL, holocytochrome c synthase CYC3, YAL039C

CYC3 - Non-Fungal Related Genes/Proteins (6)

ReferenceOther Genes Addressed
Szklarczyk R and Huynen MA  (2009) Expansion of the human mitochondrial proteome by intra- and inter-compartmental protein duplication. Genome Biol 10(11):R135
Wimplinger I, et al.  (2007) HCCS loss-of-function missense mutation in a female with bilateral microphthalmia and sclerocornea: a novel gene for severe ocular malformations? Mol Vis 13:1475-82
Wimplinger I, et al.  (2006) Mutations of the Mitochondrial Holocytochrome c-Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome. Am J Hum Genet 79(5):878-89
Bernard DG, et al.  (2003) Overlapping specificities of the mitochondrial cytochrome c and c1 heme lyases. J Biol Chem 278(50):49732-42
Schwarz QP and Cox TC  (2002) Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome c. Genomics 79(1):51-7
Schaefer L, et al.  (1996) Cloning and characterization of a putative human holocytochrome c-type synthetase gene (HCCS) isolated from the critical region for microphthalmia with linear skin defects (MLS). Genomics 34(2):166-72