| ID: 54407 | solute carrier family 38 member 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (46358188..46372773, complement) | ATA2, PRO1068, SAT2, SNAT2 | 605180 |
| ID: 5082 | phosducin like [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (122818097..122828588, complement) | PhLP | 604421 |
| ID: 8761 | poly(A) binding protein cytoplasmic 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (39560816..39576790, complement) | APP-1, APP1, PABP4, iPABP | 603407 |
| ID: 5826 | ATP binding cassette subfamily D member 4 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74285269..74302934, complement) | ABC41, EST352188, MAHCJ, P70R, P79R, PMP69, PXMP1L | 603214 |
| ID: 124936 | cytochrome b5 domain containing 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (4143168..4157701) | | |
| ID: 90576 | zinc finger protein 799 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12390016..12415084, complement) | HIT-40, HIT40, ZNF842 | 619916 |
| ID: 23479 | iron-sulfur cluster assembly enzyme [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (108561463..108569384) | 2310020H20Rik, HML, ISU2, NIFU, NIFUN, hnifU | 611911 |
| ID: 9114 | ATPase H+ transporting V0 subunit d1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (67438019..67481157, complement) | ATP6D, ATP6DV, P39, VATX, VMA6, VPATPD | 607028 |
| ID: 170622 | COMM domain containing 6 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (75525214..75549439, complement) | Acrg | 612377 |
| ID: 22928 | selenophosphate synthetase 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30443631..30445874, complement) | SPS2 | 606218 |
| ID: 7353 | ubiquitin recognition factor in ER associated degradation 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19449911..19479193, complement) | UFD1L | 601754 |
| ID: 4602 | MYB proto-oncogene, transcription factor [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (135181308..135219172) | Cmyb, c-myb, c-myb_CDS, efg | 189990 |
| ID: 10069 | RWD domain containing 2B [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (29004384..29019349, complement) | C21orf6, GL011 | 617843 |
| ID: 81550 | tudor domain containing 3 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (60395533..60573879) | | 614392 |
| ID: 7531 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (1344275..1400222, complement) | 14-3-3E, HEL2, KCIP-1, MDCR, MDS | 605066 |
| ID: 9013 | TATA-box binding protein associated factor, RNA polymerase I subunit C [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (84177855..84187057, complement) | MGC:39976, SL1, TAFI110, TAFI95 | 604905 |
| ID: 2120 | ETS variant transcription factor 6 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (11649674..11895377) | TEL, TEL/ABL, THC5 | 600618 |