Publication for Hyou1 and Pdia3

Species	Symbol	Function*	Entrez Gene ID*	Other ID	Gene coexpression	CoexViewer
mmu	Hyou1	hypoxia up-regulated 1	12282			[link]
mmu	Pdia3	protein disulfide isomerase associated 3	14827

Pubmed ID	Priority	Text
21503947	0.98	ORP150, all isoforms of PDI, catalase, GSTmu1 and GSTpi1, UCCR, cytochrome b-5, glyoxylase 1, MUPs; ADRP, FPP and L-FABP (Table S3), confirming the constitutive UPR and impaired energy metabolism at protein levels in LGKO.
22443930	0.98	ORP 150, ERp57, and others) that bear multiple low-affinity Ca2+-binding sites.
23750325	0.98	PDI, ERp72, GRP170/ORP150, CaBP1 (calcium binding protein), cyclophilin B and SDF2-L1, which processes unfolded protein substrates.
26228140	0.98	Hyou1 or ORP-150), and protein disulfide isomerase family A member 3 (Pdia3)], as well as genes involved in protein degradation, such as ER degradation-enhancing alpha-mannosidase (EDEM), and glycosylation, such as mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase (Mgat2):was readily detected in the lean samples but markedly diminished in the ob/ob hepatocytes (Fig. 1C).
29244830	0.98	Hyou1, Mthfd2, and PDI.
31527703	0.98	Hyou1, Pdia3, Pdia4 and Txndc5) are involved in the protein processing in endoplasmic reticulum (ER) pathway (KEGG identifier mmu04141, odds-ratio = 6.7, P-value = 0.002, Fisher's Exact test, see Fig. 6C), enlightening the molecular basis of the changes in ER architecture that take place during the transition from oocyte to embryo and that are concomitant to the increase in protein synthesis and folding after EGA.
31260448	0.97	Hyou1, Manf (Armet), Pdia3, Pdia4, Trib3 and Xbp1 (S1 Table).
	0.97	Hyou1, Manf, Pdia3, Pdia4, Pdia6 and Xbp1 gene expression.
22623366	0.97	ERp57, total GRP78, KDEL-positive GRP94, and ORP150 in the liver of LPS-challenged GSNOR-/- mice were reversed by further genetic deletion of iNOS (Fig. 5D).
29565997	0.96	PDIA3, CALR, GANAB and HYOU1 suggesting its functional link with protein folding and response to stress.
29666155	0.93	GRP170, the other ER NEF, showed a modest increase in expression beginning at 6 months, whereas the lectin chaperones (calnexin and calreticulin) and their cofactor, ERP57, were more robustly upregulated.
25973683	0.80	HYOU1), ERdj3 (DNAJB11) and ERdj6 (DNAJC3), the ER foldases PDIA3 (ERp57), PDIA4 (ERp70), ERp44 and FKBP7, and the N-linked glycosylation factor SDF2L1.