| ID: 9121 | solute carrier family 16 member 5 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (75087385..75110149) | MCT5, MCT6 | 603879 |
| ID: 53827 | FXYD domain containing ion transport regulator 5 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (35154735..35169881) | DYSAD, HSPC113, IWU1, KCT1, OIT2, PRO6241, RIC | 606669 |
| ID: 1831 | TSC22 domain family member 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (107713221..107775988, complement) | DIP, DSIPI, GILZ, TSC-22R | 300506 |
| ID: 11186 | Ras association domain family member 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (50329788..50340836, complement) | 123F2, NORE2AA, RDA32, REH3P21, RASSF1 | 605082 |
| ID: 860 | RUNX family transcription factor 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (45328330..45551082) | AML3, CBF-alpha-1, CBFA1, CCD, CCD1, CLCD, OSF-2, OSF2, PEA2aA, PEBP2aA | 600211 |
| ID: 89848 | FCH and double SH3 domains 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (141639302..141651418, complement) | NWK2 | 617555 |
| ID: 65010 | solute carrier family 26 member 6 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (48625723..48635461, complement) | | 610068 |
| ID: 116985 | ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (72685069..72752408, complement) | CENTD2, cnt-d2 | 606646 |