Homo sapiens proteoglycan 4 (PRG4), transcript variant A, also known a - Nucleotide

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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.
Recombinant Human Proteoglycan 4 (rhPRG4) Downregulates TNFα-Stimulated NFκB Activity and FAT10 Expression in Human Corneal Epithelial Cells. [Int J Mol Sci. 2022]
Recombinant Human Proteoglycan 4 (rhPRG4) Downregulates TNFα-Stimulated NFκB Activity and FAT10 Expression in Human Corneal Epithelial Cells.
Menon NG, Suhail Y, Goyal R, Du W, Tanguay AP, Jay GD, Ghosh M, Kshitiz, Schmidt TA. Int J Mol Sci. 2022 Oct 22; 23(21). Epub 2022 Oct 22.
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.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the PRG4 gene.
RefSeq protein product
See the reference protein sequence for proteoglycan 4 isoform A preproprotein (NP_005798.3).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide