| ID: 83758 | retinol binding protein 5 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (7115736..7130005, complement) | CRBP-III, CRBP3, CRBPIII, HRBPiso | 611866 |
| ID: 5174 | PDZ domain containing 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (145670852..145707400, complement) | CAP70, CLAMP, NHERF-3, NHERF3, PDZD1 | 603831 |
| ID: 2538 | glucose-6-phosphatase catalytic subunit 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42900799..42914438) | G6PC, G6PT, G6Pase, GSD1, GSD1a | 613742 |
| ID: 3273 | histidine rich glycoprotein [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (186666014..186678234) | HPRGP, THPH11, HRG | 142640 |
| ID: 440712 | regulator of hemoglobinization and erythroid cell expansion [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (206053173..206102449) | C1orf186 | 616088 |
| ID: 5314 | PKHD1 ciliary IPT domain containing fibrocystin/polyductin [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (51615299..52087615, complement) | ARPKD, FCYT, FPC, PCYT, PKD4, TIGM1 | 606702 |
| ID: 9154 | solute carrier family 28 member 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (84884662..84975649) | CNT1, HCNT1, URCTU | 606207 |
| ID: 10786 | solute carrier family 17 member 3 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (25844856..25874243, complement) | GOUT4, NPT4, UAQTL4 | 611034 |
| 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: 6568 | solute carrier family 17 member 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (25723743..25832052, complement) | NAPI-1, NPT-1, NPT1 | 182308 |
| ID: 1610 | D-amino acid oxidase [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (108880092..108901043) | DAAO, DAMOX, OXDA | 124050 |
| ID: 5624 | protein C, inactivator of coagulation factors Va and VIIIa [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127418427..127429242) | APC, PC1, THPH3, THPH4, PROC | 612283 |
| ID: 64902 | alanine--glyoxylate aminotransferase 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (34998102..35047949, complement) | AGT2, BAIBA, DAIBAT | 612471 |
| ID: 9 | N-acetyltransferase 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (18170467..18223689) | AAC1, MNAT, NAT-1, NATI | 108345 |
| ID: 9027 | N-acetyltransferase 8 (putative) [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (73640723..73642422, complement) | ATase2, CCNAT, CML1, GLA, Hcml1, TSC501, TSC510 | 606716 |
| ID: 51179 | hydroxyacid oxidase 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (119368785..119394130) | GIG16, HAOX2 | 605176 |