TPT1P8 Gene

Name tumor protein, translationally-controlled 1 pseudogene 8
Description Predicted to enable calcium ion binding activity. Predicted to be involved in apoptotic process. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]
Synonyms FKSG2
Proteins TCTP8_HUMAN
NCBI Gene ID 59347
API
Download Associations
Predicted Functions View TPT1P8's ARCHS4 Predicted Functions.
Co-expressed Genes View TPT1P8's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View TPT1P8's ARCHS4 Predicted Functions.

Functional Associations

TPT1P8 has 168 functional associations with biological entities spanning 4 categories (functional term, phrase or reference, disease, phenotype or trait, cell line, cell type or tissue, gene, protein or microRNA) extracted from 6 datasets.

Click the + buttons to view associations for TPT1P8 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles tissues with high or low expression of TPT1P8 gene relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles tissues with high or low expression of TPT1P8 gene relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
GEO Signatures of Differentially Expressed Genes for Gene Perturbations gene perturbations changing expression of TPT1P8 gene from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
GO Molecular Function Annotations 2023 molecular functions performed by TPT1P8 gene from the curated GO Molecular Function Annotations 2023 dataset.
HuGE Navigator Gene-Phenotype Associations phenotypes associated with TPT1P8 gene by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
MGI Mouse Phenotype Associations 2023 phenotypes of transgenic mice caused by TPT1P8 gene mutations from the MGI Mouse Phenotype Associations 2023 dataset.