| ID: 123876 | acyl-CoA synthetase medium chain family member 2A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20451521..20487669) | A-923A4.1, ACSM2 | 614358 |
| ID: 64577 | aldehyde dehydrogenase 8 family member A1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (134917393..134950101, complement) | ALDH12, DJ352A20.2 | 606467 |
| 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: 10367 | mitochondrial calcium uptake 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (72367340..72626079, complement) | CALC, CBARA1, EFHA3, MPXPS, ara CALC | 605084 |
| ID: 348158 | acyl-CoA synthetase medium chain family member 2B [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20536226..20576367, complement) | ACSM2, HXMA, HYST1046 | 614359 |
| ID: 10864 | solute carrier family 22 member 7 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (43295714..43305538) | NLT, OAT2, hOAT11 | 604995 |
| ID: 8858 | protein Z, vitamin K dependent plasma glycoprotein [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113158648..113172386) | PZ | 176895 |
| ID: 10841 | formimidoyltransferase cyclodeaminase [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46136262..46155579, complement) | LCHC1 | 606806 |
| 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: 3242 | 4-hydroxyphenylpyruvate dioxygenase [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (121839527..121888611, complement) | 4-HPPD, 4HPPD, GLOD3, HPPD, HPPDASE, PPD | 609695 |
| ID: 1582 | cytochrome P450 family 8 subfamily B member 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (42872192..42875879, complement) | CP8B, CYP12, CYPVIIIB1 | 602172 |
| ID: 9 | N-acetyltransferase 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (18170467..18223689) | AAC1, MNAT, NAT-1, NATI | 108345 |
| ID: 5091 | pyruvate carboxylase [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66848420..66958383, complement) | PCB | 608786 |
| ID: 1757 | sarcosine dehydrogenase [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133659418..133739955, complement) | BPR-2, DMGDHL1, SAR, SARD, SDH | 604455 |
| ID: 143941 | tetratricopeptide repeat domain 36 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (118527474..118530993) | HBP21 | 620701 |
| ID: 229 | aldolase, fructose-bisphosphate B [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (101420560..101435774, complement) | ALDB, ALDO2 | 612724 |
| ID: 5340 | plasminogen [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (160702193..160754097) | HAE4 | 173350 |
| ID: 1409 | crystallin alpha A [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43169008..43172810) | CRYA1, CTRCT9, HSPB4 | 123580 |
| ID: 55937 | apolipoprotein M [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31652404..31658210) | G3a, HSPC336, NG20, apo-M | 606907 |
| ID: 114571 | solute carrier family 22 member 9 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (63369785..63410294) | HOAT4, OAT4, OAT7, UST3H, ust3 | 607579 |