We have a suspicion that you are an automated web bot software, not a real user. To keep our site fast for other users, we have slowed down this page. The slowdown will gradually disappear. If you think this is a mistake, please contact us at genome-www@soe.ucsc.edu. Also note that all data for hgGeneGraph can be obtained through our public MySQL server and all our software source code is available and can be installed locally onto your own computer. If you are unsure how to use these resources, do not hesitate to contact us.
UCSC Genome Browser Gene Interaction Graph
Gene interactions and pathways from curated databases and text-mining

◀ Back to EGFR

EGFR — ERBB4

Pathways - manually collected, often from reviews:

Protein-Protein interactions - manually collected from original source literature:

Studies that report less than 10 interactions are marked with *

Text-mined interactions from Literome

Bei et al., J Pathol 2001 (Carcinoma, Squamous Cell...) : Among invasive and in situ carcinoma, EGFR expression was the most prevalent ( in 29/32 and 8/11 cases, respectively ) followed by ErbB2 ( 17/32 and 2/11 ) and ErbB4 ( 9/32 and 1/10 ), while ErbB3 was only detected in invasive tumours ( 12/32 )
Shi et al., Dev Biol 2003 (MAP Kinase Signaling System) : At the molecular level, reduced expression of epidermal growth factor receptor , attenuated protein cleavage of ErbB4 , and changes in MAPK activation were also detected in TACE ( DeltaZn/DeltaZn ) knockout heart tissues
Muraoka-Cook et al., Mol Endocrinol 2008 : We found that full prolactin mediated STAT5A activation and binding to the endogenous beta-casein promoter required ErbB4/HER4 but did not require ErbB1/epidermal growth factor receptor
Frey et al., Lab Invest 2010 (Colonic Neoplasms) : Furthermore, ErbB4 expression promoted EGFR phosphorylation in the presence of heregulin, implicating ErbB4-EGFR heterodimerization in these responses