Skip to main content
Fig. 3 | BMC Medical Genomics

Fig. 3

From: A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case

Fig. 3

Schematic representation of protein–protein interaction network of ESRRB using STRING database. Predicted functional partners are as follows: NCOA3 (Nuclear receptor coactivator), TBX3 (T-box transcription factor), POU5F1 (Putative POU domain, class 5, transcription factor 1B), SALL4 (Sal-like protein 4), NR0B1 (Nuclear receptor subfamily 0 group B member 1), TFCP2L1 (Transcription factor CP2-like protein 1), POU5F1 (POU domain, class 5, transcription factor 1), NANOG (Homeobox protein NANOG), KLF4 (Krueppel-like factor 4) and SOX2 (SRY-Box Transcription Factor 2)

Back to article page

BMC Medical Genomics

ISSN: 1755-8794

Contact us