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. 2013 Nov 5;42(3):1474–1496. doi: 10.1093/nar/gkt989

Table 1.

Endothelial disease relevant genes exposed by association to multiple TFs in HUVEC data

Symbol Pathway Entrez GeneID Number of disease Number of TFs
NOS3 Arginine and proline metabolism 4846 140 8
PTGS2 Eicosanoid metabolism 5743 97 8
HMOX1 Heme degradation 3162 56 8
ABCA1 Transport, extracellular; transport, golgi apparatus 19 20 9
PTGS1 Eicosanoid metabolism 5742 12 8
LIPG Triacylglycerol synthesis 9388 9 10
ADA Nucleotides; purine catabolism 100 9 9
PDE4D Nucleotides 5144 9 8
PDE4B Nucleotides 5142 8 9
ABCC4 Transport, extracellular 10 257 7 9
PDE3A Nucleotides 5139 7 8
PIK3CG Inositol phosphate metabolism 5294 7 8
SLC12A2 Transport, extracellular 6558 6 9
PAFAH2 Glycerophospholipid metabolism 5051 4 9
GCLM Glutathione metabolism 2730 3 10
MTHFD1L Folate metabolism 25 902 3 10
GALNT2 O-glycan biosynthesis 2590 3 9
PPAP2B Triacylglycerol synthesis 8613 1 10
NNMT NAD metabolism 4837 1 10

The 19 Recon1 metabolic genes annotated with endothelial-relevant disease terms in the DisGeNET database (32) and having an active TSS mark (H3K4me3) with putative binding of at least 8 TFs from ChIP-Seq HUVEC studies (see ‘Materials and Methods’ section for details) are presented.