| ID: 7001 | peroxiredoxin 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12796823..12801800, complement) | HEL-S-2a, NKEF-B, NKEFB, PRP, PRX2, PRXII, PTX1, TDPX1, TPX1, TSA | 600538 |
| ID: 2030 | solute carrier family 29 member 1 (Augustine blood group) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (44219615..44234142) | AUG, ENT1, hENT1 | 602193 |
| ID: 4000 | lamin A/C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156082573..156140081) | CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL, FPLD, FPLD2, HGPS, IDC, LDP1, LFP, LGMD1B, LMN1, LMNC, LMNL1, MADA, PRO1 | 150330 |
| ID: 5526 | protein phosphatase 2 regulatory subunit B'beta [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (64917573..64934475) | B56B, B56beta, PR61B | 601644 |
| ID: 25829 | transmembrane protein 184B [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38216395..38273010, complement) | C22orf5, FM08, HS5O6A, HSPC256, SLC51C2 | |
| ID: 55861 | dysbindin domain containing 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45405993..45410610) | C20orf35, CK1BP, HSMNP1 | 611453 |
| ID: 2132 | exostosin glycosyltransferase 2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (44095678..44251962) | SOTV, SSMS | 608210 |
| ID: 284252 | potassium channel tetramerization domain containing 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (26454910..26657473, complement) | C18orf5 | 613420 |
| ID: 8573 | calcium/calmodulin dependent serine protein kinase [Homo sapiens (human)] | Chromosome X, NC_000023.11 (41514934..41923554, complement) | CAGH39, CAMGUK, CMG, FGS4, LIN2, MICPCH, MRXSNA, TNRC8, hCASK | 300172 |
| ID: 285598 | ARF like GTPase 10 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (176365487..176415063) | ARL10A | |
| ID: 3730 | anosmin 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (8528874..8732137, complement) | ADMLX, HH1, HHA, KAL, KAL1, KALIG-1, KMS, WFDC19 | 300836 |
| ID: 5664 | presenilin 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (226870616..226903668) | AD3L, AD4, CMD1V, PS2, STM2 | 600759 |
| ID: 4040 | LDL receptor related protein 6 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (12116025..12267044, complement) | ADCAD2, STHAG7 | 603507 |
| ID: 84619 | zinc finger CCCH-type and G-patch domain containing [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63707442..63736142) | GPATC6, GPATCH6, KIAA1847, ZC3H9, ZC3HDC9, ZIP | 619577 |
| ID: 9751 | syntaphilin [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (1266294..1309327) | | 604942 |
| ID: 7942 | transcription factor EB [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (41683978..41736223, complement) | ALPHATFEB, BHLHE35, TCFEB | 600744 |
| ID: 64283 | Rho guanine nucleotide exchange factor 28 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (73626196..73941990) | RGNEF, RIP2, p190RHOGEF | 612790 |
| ID: 27341 | ribosomal RNA processing 7 homolog A [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (42508344..42519796, complement) | BK126B4.3, CGI-96, MCPH28, Rrp7 | 619449 |
| ID: 81493 | syncoilin, intermediate filament protein [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (32679906..32703593, complement) | SYNC1OILIN, SYNC | 611750 |
| ID: 1969 | EPH receptor A2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16124337..16156069, complement) | ARCC2, CTPA, CTPP1, CTRCT6, ECK | 176946 |