unnamed protein product [Homo sapiens]

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A needle in a haystack? The impact of a targeted epilepsy gene panel in the identification of a treatable but rapidly progressive metabolic epilepsy: CLN2 disease. [Arq Neuropsiquiatr. 2024]
A needle in a haystack? The impact of a targeted epilepsy gene panel in the identification of a treatable but rapidly progressive metabolic epilepsy: CLN2 disease.
Lourenço CM, Sallum JMF, Pereira AM, Girotto PN, Kok F, Vilela DRF, Barron E, Pessoa A, Oliveira BM. Arq Neuropsiquiatr. 2024 May; 82(5):1-8. Epub 2024 May 19.
CLN2 disease resulting from a novel homozygous deep intronic splice variant in TPP1 discovered using long-read sequencing. [Mol Genet Metab. 2023]
CLN2 disease resulting from a novel homozygous deep intronic splice variant in TPP1 discovered using long-read sequencing.
Steigerwald C, Borsuk J, Pappas J, Galey M, Scott A, Devaney JM, Miller DE, Abreu NJ. Mol Genet Metab. 2023 Dec; 140(4):107713. Epub 2023 Oct 30.
TPP1 Inhibits DNA Damage Response and Chemosensitivity in Esophageal Cancer. [Crit Rev Eukaryot Gene Expr. 2...]
TPP1 Inhibits DNA Damage Response and Chemosensitivity in Esophageal Cancer.
Wen J, Zhong X, Gao C, Yang M, Tang M, Yuan Z, Wang Q, Xu L, Ma Q, Guo X, et al. Crit Rev Eukaryot Gene Expr. 2023; 33(8):77-91.

RefSeq genomic sequence
See the genomic reference sequence for the TPP1 gene (NG_008653.1).
RefSeq protein
See the reference protein sequence for tripeptidyl-peptidase 1 preproprotein (NP_000382.3).

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Protein