ID: 100507203 | small leucine rich protein 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (130827406..130837135) | | |
ID: 727 | complement C5 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (120952335..121074865, complement) | C5Da, C5b, CPAMD4, ECLZB, C5 | 120900 |
ID: 11136 | solute carrier family 7 member 9 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (32830511..32869767, complement) | BAT1, CSNU3 | 604144 |
ID: 229 | aldolase, fructose-bisphosphate B [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (101420560..101435774, complement) | ALDB, ALDO2 | 612724 |
ID: 1757 | sarcosine dehydrogenase [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133659418..133739955, complement) | BPR-2, DMGDHL1, SAR, SARD, SDH | 604455 |
ID: 8858 | protein Z, vitamin K dependent plasma glycoprotein [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113158648..113172386) | PZ | 176895 |
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: 58510 | proline dehydrogenase 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (35799988..35812845, complement) | HSPOX1, HYPDH | 616377 |
ID: 10864 | solute carrier family 22 member 7 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (43295714..43305538) | NLT, OAT2, hOAT11 | 604995 |
ID: 64816 | cytochrome P450 family 3 subfamily A member 43 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (99828013..99866093) | | 606534 |
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: 114571 | solute carrier family 22 member 9 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (63369785..63410294) | HOAT4, OAT4, OAT7, UST3H, ust3 | 607579 |
ID: 2155 | coagulation factor VII [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113105788..113120685) | SPCA | 613878 |
ID: 8529 | cytochrome P450 family 4 subfamily F member 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (15878023..15898074, complement) | CPF2 | 604426 |
ID: 10841 | formimidoyltransferase cyclodeaminase [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46136262..46155579, complement) | LCHC1 | 606806 |
ID: 2243 | fibrinogen alpha chain [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (154583126..154590742, complement) | AMYLD2, Fib2 | 134820 |
ID: 143941 | tetratricopeptide repeat domain 36 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (118527474..118530993) | HBP21 | 620701 |
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: 55937 | apolipoprotein M [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31652404..31658210) | G3a, HSPC336, NG20, apo-M | 606907 |
ID: 199920 | FYN binding protein 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (56718789..56826914, complement) | ARAP, C1orf168 | 618478 |