| GENE NAME | PRMT7 |
| CHROMOSOME | 16 |
| ENSEMBL ID | ENSG00000132600 |
| ENTREZ ID | 54496 |
| UNIPROT ACCESSION NUMBER | Q9NVM4 |
| GO MOLECULAR FUNCTION | protein binding; histone-arginine N-methyltransferase activity; [myelin basic protein]-arginine N-methyltransferase activity; protein-arginine omega-N monomethyltransferase activity; histone binding; histone methyltransferase activity (H4-R3 specific); protein-arginine omega-N symmetric methyltransferase activity; ribonucleoprotein complex binding; S-adenosylmethionine-dependent methyltransferase activity |
| ESSENTIAL IN MOUSE | None |
| PATHWAYS | R-HSA-3214858; R-HSA-3247509; R-HSA-4839726 |
| 1 combination linked to PRMT7 | OLI1028 |
| 1 variant linked to PRMT7 | PRMT7:c.1097G>A, p.Cys366Tyr |
| 1 disease linked to PRMT7 | Short stature-brachydactyly-obesity-global developmental delay syndrome |