| P594 | Ensembl gene ID | ENSG00000238419 |
| P704 | Ensembl transcript ID | ENST00000458818 |
| P351 | Entrez Gene ID | 106480363 |
| P2888 | exact match | http://identifiers.org/ncbigene/106480363 |
| P353 | HGNC gene symbol | RNU7-186P |
| P354 | HGNC ID | 45720 |
| P2892 | UMLS CUI | C3539239 |
| P1057 | chromosome | human chromosome 17 | Q220677 |
| P4196 | cytogenetic location | 17q21.32 | |
| P5572 | expressed in | monocyte | Q107244 |
| appendix | Q9656 | ||
| right coronary artery | Q429285 | ||
| left lobe of thyroid gland | Q66508049 | ||
| muscle layer of sigmoid colon | Q66511231 | ||
| Descending thoracic aorta | Q66592966 | ||
| ascending aorta | Q2349469 | ||
| tibial arteries | Q7800442 | ||
| endometrium | Q839508 | ||
| placenta | Q1212935 | ||
| P703 | found in taxon | Homo sapiens | Q15978631 |
| P645 | genomic end | 47259420 | |
| P644 | genomic start | 47259358 | |
| P2548 | strand orientation | reverse strand | Q22809711 |
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