ID: 153527 | zinc finger matrin-type 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (140700447..140706686) | Ptg-12, Snu23 | 619930 |
ID: 51362 | cell division cycle 40 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (110180427..110232232) | EHB3, PCH15, PRP17, PRPF17 | 605585 |
ID: 54901 | CDK5 regulatory subunit associated protein 1 like 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (20534457..21232404) | | 611259 |
ID: 80306 | mediator complex subunit 28 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (17614641..17634105) | 1500003D12Rik, EG1, magicin | 610311 |
ID: 5431 | RNA polymerase II subunit B [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (56978896..57031158) | POL2RB, RPB2, hRPB140 | 180661 |
ID: 25983 | neuroguidin [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (23469703..23478826) | C14orf120, CANu1, LCP5, NGD, lpd-2 | 610777 |
ID: 29796 | ubiquinol-cytochrome c reductase, complex III subunit X [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29767369..29770413) | HSPC051, HSPC119, HSPC151, QCR9, UCCR7.2, UCRC | 610843 |
ID: 55161 | transmembrane protein 33 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (41935137..41960803) | 1600019D15Rik, Pom33, SHINC-3, SHINC3 | 618515 |
ID: 200895 | dihydrofolate reductase 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (94057922..94063320, complement) | DHFRL1, DHFRP4 | 616588 |
ID: 11017 | small nuclear ribonucleoprotein U4/U6.U5 subunit 27 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (69893956..69905236) | 27K, RY1 | 619629 |
ID: 51602 | NOP58 ribonucleoprotein [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (202265763..202303661) | HSPC120, NOP5, NOP5/NOP58 | 616742 |
ID: 1350 | cytochrome c oxidase subunit 7C [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (86617941..86620962) | | 603774 |
ID: 353088 | zinc finger protein 429 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (21505602..21540668) | | |
ID: 9487 | phosphatidylinositol glycan anchor biosynthesis class L [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16217210..16326411) | CHIME | 605947 |
ID: 440138 | ALG11 alpha-1,2-mannosyltransferase [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (52012398..52033600) | CDG1P, GT8 | 613666 |