Species	Reference gene ID	Possible function	Papers / DOI
Arabidopsis	At4g37850	Transcription factor bHLH25.	No verified direct reference in this release
Arabidopsis	At2g22750	Transcription factor bHLH18.	No verified direct reference in this release
Arabidopsis	At2g22760	Transcription factor bHLH19.	No verified direct reference in this release
Arabidopsis	At2g22770	Transcription activator that regulates the expression of at least NAI2, PYK10 and PBP1.	A novel ER-derived compartment, the ER body, selectively accumulates a beta-glucosidase with an ER-retention signal in Arabidopsis.; 2003; DOI: 10.1046/j.1365-313x.2003.01636.x; PMID: 12581307; https://pubmed.ncbi.nlm.nih.gov/12581307/ | NAI1 gene encodes a basic-helix-loop-helix-type putative transcription factor that regulates the formation of an endoplasmic reticulum-derived structure, the ER body.; 2004; DOI: 10.1105/tpc.021154; PMID: 15155889; https://pubmed.ncbi.nlm.nih.gov/15155889/ | Activation of an ER-body-localized beta-glucosidase via a cytosolic binding partner in damaged tissues of Arabidopsis thaliana.; 2005; DOI: 10.1093/pcp/pci126; PMID: 15919674; https://pubmed.ncbi.nlm.nih.gov/15919674/ | PYK10, a beta-glucosidase located in the endoplasmatic reticulum, is crucial for the beneficial interaction between Arabidopsis thaliana and the endophytic fungus Piriformospora indica.; 2008; DOI: 10.1111/j.1365-313x.2008.03424.x; PMID: 18248598; https://pubmed.ncbi.nlm.nih.gov/18248598/ | Antagonistic jacalin-related lectins regulate the size of ER body-type beta-glucosidase complexes in Arabidopsis thaliana.; 2008; DOI: 10.1093/pcp/pcn075; PMID: 18467340; https://pubmed.ncbi.nlm.nih.gov/18467340/ | NAI2 is an endoplasmic reticulum body component that enables ER body formation in Arabidopsis thaliana.; 2008; DOI: 10.1105/tpc.108.059345; PMID: 18780803; https://pubmed.ncbi.nlm.nih.gov/18780803/
Arabidopsis	At1g32640	Transcriptional activator.	Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) function as transcriptional activators in abscisic acid signaling.; 2003; DOI: 10.1105/tpc.006130; PMID: 12509522; https://pubmed.ncbi.nlm.nih.gov/12509522/ | JASMONATE-INSENSITIVE1 encodes a MYC transcription factor essential to discriminate between different jasmonate-regulated defense responses in Arabidopsis.; 2004; DOI: 10.1105/tpc.022319; PMID: 15208388; https://pubmed.ncbi.nlm.nih.gov/15208388/ | A basic helix-loop-helix transcription factor in Arabidopsis, MYC2, acts as a repressor of blue light-mediated photomorphogenic growth.; 2005; DOI: 10.1105/tpc.105.032060; PMID: 15923349; https://pubmed.ncbi.nlm.nih.gov/15923349/ | Characterization of JAZ-interacting bHLH transcription factors that regulate jasmonate responses in Arabidopsis.; 2011; DOI: 10.1093/jxb/erq408; PMID: 21321051; https://pubmed.ncbi.nlm.nih.gov/21321051/ | The Arabidopsis bHLH transcription factors MYC3 and MYC4 are targets of JAZ repressors and act additively with MYC2 in the activation of jasmonate responses.; 2011; DOI: 10.1105/tpc.110.080788; PMID: 21335373; https://pubmed.ncbi.nlm.nih.gov/21335373/ | The basic helix-loop-helix transcription factor MYC2 directly represses PLETHORA expression during jasmonate-mediated modulation of the root stem cell niche in Arabidopsis.; 2011; DOI: 10.1105/tpc.111.089870; PMID: 21954460; https://pubmed.ncbi.nlm.nih.gov/21954460/ | Arabidopsis MYC2 interacts with DELLA proteins in regulating sesquiterpene synthase gene expression.; 2012; DOI: 10.1105/tpc.112.098749; PMID: 22669881; https://pubmed.ncbi.nlm.nih.gov/22669881/ | Arabidopsis basic helix-loop-helix transcription factors MYC2, MYC3, and MYC4 regulate glucosinolate biosynthesis, insect performance, and feeding behavior.; 2013; DOI: 10.1105/tpc.113.115139; PMID: 23943862; https://pubmed.ncbi.nlm.nih.gov/23943862/ | Role of arabidopsis MYC and MYB homologs in drought- and abscisic acid-regulated gene expression.; 1997; DOI: 10.1105/tpc.9.10.1859; PMID: 9368419; https://pubmed.ncbi.nlm.nih.gov/9368419/