Tel: 1-631-626-9181 (USA)   44-207-097-1828 (Europe)
  Email:

HCCS

Official Full Name
holocytochrome c synthase
Background
The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7). Three transcript variants encoding the same protein have been found for this gene.
Synonyms
HCCS; holocytochrome c synthase; holocytochrome c synthase (cytochrome c heme lyase); cytochrome c-type heme lyase; CCHL; cytochrome c heme lyase; OTTHUMP00000022904; OTTHUMP00000022905; DKFZp779I1858; EC 4.4.1.17; Holocytochrome c type synthase; MCOPS7; OTTHUMP00000022903; OTTMUSP00000021173; OTTMUSP00000021174; RGD1563855; RP23-37L2.1; cytochrome c heme-lyase; holocytochrome c-type synthase; holocytochrome c synthase (cytochrome c heme-lyase)

Interested in learning more?

Contact us today for a free consultation with the scientific team and discover how Creative Biogene can be a valuable resource and partner for your organization.

Request a quote today!