| Gene/protein identifiers | Reported function/localization | Splicing / isoform frequency | Poly(A) tail length observation | Statistical test | Evidence type | Key source (date, DOI, URL) | Notes / limitations |
|---|---|---|---|---|---|---|---|
| *Schizosaccharomyces pombe* **tam10**; systematic ID **SPBC14C8.19**; UniProt **G2TRQ9**; protein described in the retrieved evidence as a **nucleolar RNA-binding protein implicated in mRNA processing** (pqac-00000000) | Nucleolar; implicated in mRNA processing; no enzymatic activity or pathway mechanism was directly established in the retrieved paper (pqac-00000000) | An **intron-retained (IR) isoform** of *tam10* was detected and accounted for **~18% of reads** in direct RNA sequencing (pqac-00000000, pqac-00000001) | The **IR isoform has a significantly longer poly(A) tail** than the reference isoform; this is shown specifically for *tam10* in Figure 4D (pqac-00000000, pqac-00000001) | **Wilcoxon test**; significance annotated as **\*\*\* P < 10^-5** for the comparison described in the study excerpt (pqac-00000000) | **Oxford Nanopore direct RNA sequencing (dRNA-seq)** with isoform-resolved poly(A) tail analysis; figure-based support for *tam10* comparison in Fig. 4D (pqac-00000000, pqac-00000001) | Montañés JC, Huertas M, Moro SG, Blevins WR, Carmona M, Ayté J, Hidalgo E, Albà MM. **2022-05**. *Genome Research* 32:1215-1227. **DOI:** 10.1101/gr.276516.121. **URL:** https://doi.org/10.1101/gr.276516.121 (pqac-00000000) | Current retrieved evidence is **limited to one directly relevant source**. The paper supports localization/functional description and isoform behavior, but does **not** provide detailed biochemical function, substrate specificity, interaction mechanism, or phenotype analysis for *tam10* specifically; no 2023-2024 tam10-specific study was retrieved here (pqac-00000000) |


*Table: This table condenses the currently retrieved, directly relevant evidence for *S. pombe* tam10/SPBC14C8.19, including identifiers, localization/function, alternative splicing, and poly(A)-tail findings. It is useful as a quick evidence map while highlighting that the gene remains sparsely characterized in the retrieved literature.*