Publication for Ebp and Fdps

Species	Symbol	Function*	Entrez Gene ID*	Other ID	Gene coexpression	CoexViewer
mmu	Ebp	phenylalkylamine Ca2+ antagonist (emopamil) binding protein	13595			[link]
mmu	Fdps	farnesyl diphosphate synthetase	110196

Pubmed ID	Priority	Text
30271348	0.98	Fdps (farnesyl diphosphate synthetase), Sqle (squalene epoxidase), Lss (lanosterol synthase), Dhcr24 (24-dehydrocholesterol reductase), Cyp51, Nsdhl (NAD(P) dependent steroid dehydrogenase-like), Hsd17b7, Ebp, Sc5d, and Dhcr7] exhibited reduced expression compared to ad libitum mice (Figure 8A).
	0.93	Fdps, Cyp51, Nsdhl, and Ebp were even higher expressed after 21 h refeeding compared to the corresponding starvation period at ZT 12.
19197803	0.98	Fdps, Sqle, Cyp51, Sc4mol and Ebp, are highly expressed in cumulus cells but not oocytes, thus suggesting that mouse oocytes lack the full enzymatic system required for synthesizing cholesterol.
29361464	0.83	Ebp, Fdps, Nsdhl, Pmvk, Sqle, Thrsp, Tm7sf2) and novel cholesterol genes (e.g. Acot1, Acot2, Elovl6, and Gpam) that were found by were also identified as KDs in our study for lipid and fatty acid metabolism and mitotic cell cycle-related pathways.