ID: 11169 | WD repeat and HMG-box DNA binding protein 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (54938949..55027099, complement) | AND-1, AND1, CHTF4, CTF4 | 608126 |
ID: 122809 | suppressor of cytokine signaling 4 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (55027236..55049489) | SOCS7 | 616337 |
ID: 5932 | RB binding protein 8, endonuclease [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (22914139..23026486) | COM1, CTIP, JAWAD, JWDS, RIM, SAE2, SCKL2 | 604124 |
ID: 10615 | sperm associated antigen 5 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28577574..28599025, complement) | DEEPEST, MAP126, hMAP126 | 615562 |
ID: 5888 | RAD51 recombinase [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (40694733..40732340) | BRCC5, FANCR, HRAD51, HsRad51, HsT16930, MRMV2A, RECA, RAD51 | 179617 |
ID: 83986 | family with sequence similarity 234 member A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (234821..269963) | C16orf9, ITFG3, gs19 | |
ID: 79447 | PAXIP1 associated glutamate rich protein 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (29816152..29822489) | C16orf53, GAS, PA1 | 612033 |
ID: 23592 | LEM domain containing 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (65169583..65248355) | MAN1 | 607844 |
ID: 55815 | translin associated factor X interacting protein 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (67806889..67828068) | TXI1 | 607720 |
ID: 284086 | NIMA related kinase 8 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28728788..28743455) | JCK, NEK12A, NPHP9, PKD8, RHPD2 | 609799 |
ID: 284403 | WD repeat domain 62 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (36054897..36111145) | C19orf14, MCPH2 | 613583 |
ID: 84314 | transmembrane protein 107 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (8172457..8176380, complement) | GRVS638, JBTS29, MKS13, PRO1268 | 616183 |
ID: 9837 | GINS complex subunit 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25407673..25448563) | IMD55, PSF1 | 610608 |
ID: 10400 | phosphatidylethanolamine N-methyltransferase [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (17505563..17592142, complement) | PEAMT, PEMPT2, PLMT, PNMT, PEMT | 602391 |
ID: 390637 | GDP-D-glucose phosphorylase 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (90234209..90245811) | C15orf58, VTC2 | 619240 |
ID: 64318 | NOC3 like DNA replication regulator [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (94314907..94362939, complement) | AD24, C10orf117, FAD24 | 610769 |
ID: 10497 | unc-13 homolog B [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35162009..35405335) | MUNC13, UNC13, Unc13h2, munc13-2 | 605836 |
ID: 8021 | nucleoporin 214 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (131125586..131234663) | CAIN, CAN, IIAE9 | 114350 |
ID: 5781 | protein tyrosine phosphatase non-receptor type 11 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (112418947..112509918) | BPTP3, CFC, JMML, METCDS, NS1, PTP-1D, PTP2C, SH-PTP2, SH-PTP3, SHP2 | 176876 |
ID: 158 | adenylosuccinate lyase [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (40346500..40387527) | AMPS, ASASE, ASL | 608222 |