| ID: 1757 | sarcosine dehydrogenase [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133659418..133739955, complement) | BPR-2, DMGDHL1, SAR, SARD, SDH | 604455 |
| ID: 5345 | serpin family F member 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (1742871..1755265) | A2AP, AAP, ALPHA-2-PI, API, PLI, alpha2AP | 613168 |
| ID: 9970 | nuclear receptor subfamily 1 group I member 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (161229669..161238203, complement) | CAR, CAR1, MB67 | 603881 |
| ID: 10246 | solute carrier family 17 member 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (25912754..25930691, complement) | NPT3 | 611049 |
| ID: 58510 | proline dehydrogenase 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (35799988..35812845, complement) | HSPOX1, HYPDH | 616377 |
| ID: 420 | ADP-ribosyltransferase 4 (inactive) (Dombrock blood group) [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (14825569..14843526, complement) | ARTC4, CD297, DO, DO/ART4, DOK1 | 110600 |
| ID: 199920 | FYN binding protein 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (56718789..56826914, complement) | ARAP, C1orf168 | 618478 |
| ID: 8858 | protein Z, vitamin K dependent plasma glycoprotein [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113158648..113172386) | PZ | 176895 |
| ID: 64816 | cytochrome P450 family 3 subfamily A member 43 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (99828013..99866093) | | 606534 |
| ID: 1369 | carboxypeptidase N subunit 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (100042193..100081869, complement) | CPN, SCPN | 603103 |
| ID: 3026 | hyaluronan binding protein 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (113550831..113589602) | FSAP, HABP, HGFAL, NMTC5, PHBP | 603924 |
| ID: 3053 | serpin family D member 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (20774113..20787720) | D22S673, HC2, HCF2, HCII, HLS2, LS2, THPH10 | 142360 |
| ID: 114571 | solute carrier family 22 member 9 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (63369785..63410294) | HOAT4, OAT4, OAT7, UST3H, ust3 | 607579 |
| ID: 388646 | guanylate binding protein 7 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (89131742..89176003, complement) | GBP4L | 612468 |
| ID: 10864 | solute carrier family 22 member 7 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (43295714..43305538) | NLT, OAT2, hOAT11 | 604995 |
| ID: 727 | complement C5 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (120952335..121074865, complement) | C5Da, C5b, CPAMD4, ECLZB, C5 | 120900 |
| ID: 6360 | C-C motif chemokine ligand 16 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (35976499..35981497, complement) | CKb12, HCC-4, ILINCK, LCC-1, LEC, LMC, Mtn-1, NCC-4, NCC4, SCYA16, SCYL4 | 601394 |
| ID: 6580 | solute carrier family 22 member 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (160121815..160158718) | HOCT1, OCT1, oct1_cds | 602607 |
| ID: 10367 | mitochondrial calcium uptake 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (72367340..72626079, complement) | CALC, CBARA1, EFHA3, MPXPS, ara CALC | 605084 |
| ID: 2147 | coagulation factor II, thrombin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (46719213..46739506) | PT, RPRGL2, THPH1 | 176930 |