| ID: 84647 | phospholipase A2 group XIIB [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (72934762..72954806, complement) | FKSG71, GXIIB, GXIIIsPLA2, PLA2G13, sPLA2-GXIIB | 611653 |
| ID: 229 | aldolase, fructose-bisphosphate B [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (101420560..101435774, complement) | ALDB, ALDO2 | 612724 |
| ID: 55937 | apolipoprotein M [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31652404..31658210) | G3a, HSPC336, NG20, apo-M | 606907 |
| ID: 389643 | nuclear GTPase, germinal center associated [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (28021964..28083936, complement) | C8orf80, HMFN0672, SLIP-GC, SLIPGC | 619088 |
| ID: 143941 | tetratricopeptide repeat domain 36 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (118527474..118530993) | HBP21 | 620701 |
| ID: 2938 | glutathione S-transferase alpha 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (52791371..52803816, complement) | GST-epsilon, GST2-1, GTH1, GSTA1 | 138359 |
| ID: 100507203 | small leucine rich protein 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (130827406..130837135) | | |
| ID: 2939 | glutathione S-transferase alpha 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (52750087..52763475, complement) | GST2-2, GTA2, GTH2, GSTA2 | 138360 |
| ID: 1579 | cytochrome P450 family 4 subfamily A member 11 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (46929188..46941476, complement) | CP4Y, CYP4A2, CYP4AII, CYPIVA11 | 601310 |
| ID: 11136 | solute carrier family 7 member 9 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32830511..32869767, complement) | BAT1, CSNU3 | 604144 |
| ID: 9971 | nuclear receptor subfamily 1 group H member 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (100473866..100564414) | BAR, FXR, HRR-1, HRR1, PFIC5, RIP14 | 603826 |
| ID: 727 | complement C5 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (120952335..121074865, complement) | C5Da, C5b, CPAMD4, ECLZB, C5 | 120900 |
| ID: 440712 | regulator of hemoglobinization and erythroid cell expansion [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (206053173..206102449) | C1orf186 | 616088 |