Gene | NOP2 |
Biotype | protein_coding |
Description | NOP2 nucleolar protein |
Synonyms | NOL1; NOP120; NSUN1; p120; |
Location | chr12:6556863-6568691 |
Ensembl | ENSG00000111641 |
Entrez | 4839 |
Hgnc | 7867 |
Hprd | 01244 |
Mim | 164031 |
Swissprot | P46087 |
Trembl | F5GYR3 F5H5X6 F5H709 F5H8G6 F5GWB7 F5H359 A0A087WV73 |
Vega | OTTHUMG00000169163 |
Studies containing regions of association that span this gene are shown below. Please note that when making comparisons across studies, that they may vary in terms of size, genotyping platform, and exclusion criteria. If the 'Odds Ratio' is less than 1 then the region is protective (alleles are marked as blue) otherwise it is susceptible (alleles marked as red).
Study | Publication | Disease | Region | Marker | Alleles | P-value | OR | MAF | Gene(s) |
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Gene sets for the gene NOP2 are derived from MSigDB
Name | Genes |
---|
Organism | Gene | Phenotype | Resources |
---|---|---|---|
Mouse | MGI:107891 | MGI:107891 | IMPC |