| ID: 3614 | inosine monophosphate dehydrogenase 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (128392277..128409982, complement) | IMPD, IMPD1, IMPDH-I, LCA11, RP10, sWSS2608 | 146690 |
| ID: 129303 | transmembrane protein 150A [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (85598547..85602698, complement) | TM6P1, TMEM150, TTN1 | 616757 |
| ID: 8884 | solute carrier family 5 member 6 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27199587..27212787, complement) | COMNB, NERIB, SMVT, SMVTD, hSMVT | 604024 |
| ID: 64224 | HERPUD family member 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (35632659..35695135, complement) | | 620829 |
| ID: 51374 | all-trans retinoic acid induced differentiation factor [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27212041..27217183) | APR--3, APR-3, APR3, C2orf28, HSPC013, PRO240, p18 | 619682 |
| ID: 1181 | chloride voltage-gated channel 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (184346185..184361605, complement) | CIC-2, CLC2, ECA2, ECA3, EGI11, EGI3, EGMA, EJM6, EJM8, FHA2, FHII, HALD2, LKPAT, clC-2 | 600570 |
| ID: 9031 | bromodomain adjacent to zinc finger domain 1B [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (73440406..73522293, complement) | WBSCR10, WBSCR9, WSTF | 605681 |
| ID: 5437 | RNA polymerase II, I and III subunit H [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (184361710..184368591) | RPABC3, RPB17, RPB8 | 606023 |
| ID: 2222 | farnesyl-diphosphate farnesyltransferase 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (11795582..11839298) | DGPT, ERG9, SQS, SQSD, SS | 184420 |
| ID: 25909 | AT-hook containing transcription factor 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (246839098..246931948, complement) | ELYS, MST108, MSTP108, TMBS62 | 610853 |
| ID: 79837 | phosphatidylinositol-5-phosphate 4-kinase type 2 gamma [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (57591192..57603418) | PIP5K2C | 617104 |
| ID: 2956 | mutS homolog 6 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (47783145..47810101) | GTBP, GTMBP, HNPCC5, HSAP, LYNCH5, MMRCS3, MSH-6, p160 | 600678 |
| ID: 993 | cell division cycle 25A [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (48157146..48188417, complement) | CDC25A2 | 116947 |
| ID: 4831 | NME/NM23 nucleoside diphosphate kinase 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (51165536..51171744) | NDKB, NDPK-B, NDPKB, NM23-H2, NM23B, PUF | 156491 |
| ID: 152002 | xyloside xylosyltransferase 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (195068284..195271159, complement) | C3orf21 | 614552 |
| ID: 29929 | ALG6 alpha-1,3-glucosyltransferase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (63367627..63438553) | CDG1C | 604566 |
| ID: 10427 | SEC24 homolog B, COPII coat complex component [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (109433815..109540896) | SEC24 | 607184 |
| ID: 91010 | formin like 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (49636499..49707405, complement) | FHOD3, FRL2, WBP-3, WBP3 | 616288 |
| ID: 56255 | thioredoxin related transmembrane protein 4 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (7977346..8019761, complement) | DJ971N18.2, PDIA14, TXNDC13 | 616766 |
| ID: 374291 | NADH:ubiquinone oxidoreductase core subunit S7 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (1383907..1395584) | CI-20, CI-20KD, MC1DN3, MY017, PSST | 601825 |