Among these, PSMG3 exhibited the highest expression (gene ID: 84262; updated on July 15, 2015; gene type: protein-coding; species: Homo sapiens; alias: C7orf48 or PAC3; other sources: Ensemble: ENSG 00000157778, HPRD: 14404, and Vega: OTTHUMG00000119043; related diseases: neoplasms, autistic disorder, fibrosis, growth disorders, liver diseases, shock; related IncRNA: LINC01561 and ZRANB2-AS2; targeted miRNA: hsa-miR-92a-3p). Here, PSMG3 is linked to hereditary endocrine growth disease.