P594 | Ensembl gene ID | ENSG00000278331 |
P704 | Ensembl transcript ID | ENST00000621869 |
P351 | Entrez Gene ID | 106479635 |
P2888 | exact match | http://identifiers.org/ncbigene/106479635 |
P353 | HGNC gene symbol | RNU6-156P |
P354 | HGNC ID | 47119 |
P2892 | UMLS CUI | C3816332 |
P1057 | chromosome | human chromosome 9 | Q840604 |
P4196 | cytogenetic location | 9p11.2 | |
P5572 | expressed in | monocyte | Q107244 |
hypothalamus | Q164386 | ||
Descending thoracic aorta | Q66592966 | ||
blood | Q7873 | ||
left ventricle | Q876089 | ||
ascending aorta | Q2349469 | ||
left coronary artery | Q744391 | ||
subcutaneous adipose tissue | Q30015788 | ||
muscle layer of sigmoid colon | Q66511231 | ||
mucosa of esophagus | Q66559451 | ||
P703 | found in taxon | Homo sapiens | Q15978631 |
P645 | genomic end | 40759706 | |
P644 | genomic start | 40759600 | |
P2548 | strand orientation | reverse strand | Q22809711 |