ID: 112479 | ERI1 exoribonuclease family member 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20780193..20806472, complement) | EXOD1, ZGRF5 | |
ID: 81691 | RNA exonuclease 5 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20806425..20849665) | NEF-sp | |
ID: 84896 | ATPase family AAA domain containing 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (87751512..87841361, complement) | AFDC1, FNP001, HKPX4, Msp1, THORASE, hATAD1 | 614452 |
ID: 9236 | cell cycle progression 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (55355239..55408359, complement) | CPR8 | 611326 |
ID: 57109 | REX4 homolog, 3'-5' exonuclease [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (133406058..133418172, complement) | REX4, XPMC2, XPMC2H | 602930 |
ID: 28991 | COMM domain containing 5 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144837978..144853556, complement) | HCARG, HT002 | 608216 |
ID: 51004 | coenzyme Q6, monooxygenase [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (73949926..73963670) | CGI-10, CGI10, COQ10D6 | 614647 |
ID: 83985 | SPNS lysolipid transporter 1, lysophospholipid [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (28974778..28984765) | HSpin1, LAT, PP2030, SLC62A1, SLC63A1, SPIN1, SPINL, nrs | 612583 |
ID: 146434 | zinc finger protein 597 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (3432414..3443504, complement) | HIT-4 | 614685 |
ID: 55775 | tyrosyl-DNA phosphodiesterase 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (89954968..90044764) | | 607198 |
ID: 124045 | spermatogenesis associated 33 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89657776..89670458) | C16orf55 | 615409 |
ID: 7181 | nuclear receptor subfamily 2 group C member 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95020229..95073618, complement) | TR2 | 601529 |
ID: 23560 | GTP binding protein 4 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (988434..1019932) | CRFG, NGB, NOG1 | 619169 |
ID: 23589 | calcium regulated heat stable protein 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (8852942..8869006, complement) | CRHSP-24, CRHSP24, CSDC1 | 616885 |
ID: 64779 | methenyltetrahydrofolate synthetase domain containing [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (86530186..86555235, complement) | | 616820 |
ID: 84314 | transmembrane protein 107 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (8172457..8176380, complement) | GRVS638, JBTS29, MKS13, PRO1268 | 616183 |
ID: 8836 | gamma-glutamyl hydrolase [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (63015079..63038806, complement) | GATD10, GH | 601509 |
ID: 79738 | Bardet-Biedl syndrome 10 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (76344474..76348415, complement) | C12orf58 | 610148 |
ID: 51001 | mitochondrial transcription termination factor 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (96239398..96261613, complement) | CGI-12, MTERFD1 | 616930 |
ID: 58485 | trafficking protein particle complex subunit 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7930345..7931999, complement) | BET5, MUM2 | 610969 |