RecName: Full=Proteoglycan 4; AltName: Full=Lubricin; AltName: Full=Me - Protein

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A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report. [Pediatr Rheumatol Online J. 2023]
A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report.
Bağrul İ, Ceylaner S, Yildiz YT, Tuncez S, Aydin EA, Bağlan E, Ozdel S, Bülbül M. Pediatr Rheumatol Online J. 2023 Jan 24; 21(1):8. Epub 2023 Jan 24.
Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome: The First Familial Case in China and Novel Mutations of the Proteoglycan 4 Gene. [J Rheumatol. 2022]
Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome: The First Familial Case in China and Novel Mutations of the Proteoglycan 4 Gene.
Zhang JM, Gao FQ, Li CF, Kuang WY, Deng JH, Tan XH, Li C, Li SP. J Rheumatol. 2022 Dec; 49(12):1400-1402. Epub 2022 Sep 15.
Recombinant Human Proteoglycan 4 Regulates Phagocytic Activation of Monocytes and Reduces IL-1β Secretion by Urate Crystal Stimulated Gout PBMCs. [Front Immunol. 2021]
Recombinant Human Proteoglycan 4 Regulates Phagocytic Activation of Monocytes and Reduces IL-1β Secretion by Urate Crystal Stimulated Gout PBMCs.
ElSayed S, Jay GD, Cabezas R, Qadri M, Schmidt TA, Elsaid KA. Front Immunol. 2021; 12:771677. Epub 2021 Dec 21.

RefSeq genomic sequence
See the genomic reference sequence for the PRG4 gene (NG_008248.2).
RefSeq protein isoforms
See 5 reference sequence protein isoforms for the PRG4 gene.

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