tripeptidyl-peptidase 2 isoform X1 [Homo sapiens]

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Immune deficiency, autoimmune disease and intellectual disability: A pleiotropic disorder caused by biallelic variants in the TPP2 gene. [Clin Genet. 2021]
Immune deficiency, autoimmune disease and intellectual disability: A pleiotropic disorder caused by biallelic variants in the TPP2 gene.
Atallah I, Quinodoz M, Campos-Xavier B, Peter VG, Fouriki A, Bonvin C, Bottani A, Kumps C, Angelini F, Bellutti Enders F, et al. Clin Genet. 2021 Jun; 99(6):780-788. Epub 2021 Feb 21.
TPP2 mutation associated with sterile brain inflammation mimicking MS. [Neurol Genet. 2018]
TPP2 mutation associated with sterile brain inflammation mimicking MS.
Reinthaler EM, Graf E, Zrzavy T, Wieland T, Hotzy C, Kopecky C, Pferschy S, Schmied C, Leutmezer F, Keilani M, et al. Neurol Genet. 2018 Dec; 4(6):e285. Epub 2018 Nov 13.
Dual proteolytic pathways govern glycolysis and immune competence. [Cell. 2014]
Dual proteolytic pathways govern glycolysis and immune competence.
Lu W, Zhang Y, McDonald DO, Jing H, Carroll B, Robertson N, Zhang Q, Griffin H, Sanderson S, Lakey JH, et al. Cell. 2014 Dec 18; 159(7):1578-90.

RefSeq genomic sequence
See the genomic reference sequence for the TPP2 gene (NG_063544.1).
RefSeq mRNA
See reference mRNA sequence for the TPP2 gene (XM_005254070.3).
RefSeq protein isoforms
See 12 reference sequence protein isoforms for the TPP2 gene.

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Protein