ID: 1678 | translocase of inner mitochondrial membrane 8A [Homo sapiens (human)] | Chromosome X, NC_000023.11 (101345661..101348742, complement) | DDP, DDP1, DFN1, MTS, TIM8 | 300356 |
ID: 64789 | exonuclease 5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (40508767..40516038) | C1orf176, DEM1, Exo V, hExo5 | 618601 |
ID: 5921 | RAS p21 protein activator 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (87267883..87391916) | CM-AVM, CMAVM, CMAVM1, GAP, PKWS, RASA, RASGAP, p120, p120GAP, p120RASGAP | 139150 |
ID: 84306 | programmed cell death 2 like [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (34404399..34426168) | | 615661 |
ID: 3985 | LIM domain kinase 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (31212298..31280080) | | 601988 |
ID: 390980 | zinc finger protein 805 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (57240632..57262728) | | |
ID: 81608 | factor interacting with PAPOLA and CPSF1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (53377641..53460862) | FIP1, Rhe, hFip1 | 607686 |
ID: 84068 | solute carrier family 10 member 7 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (146253981..146521940, complement) | C4orf13, P7, SSASKS | 611459 |
ID: 9553 | mitochondrial ribosomal protein L33 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27771719..27779733) | C2orf1, L33mt, MRP-L33, RPL33L, bL33m | 610059 |
ID: 51566 | armadillo repeat containing X-linked 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (101623151..101627843) | ALEX3, GASP6, dJ545K15.2 | 300364 |
ID: 57711 | zinc finger protein 529 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (36543613..36605543, complement) | | |
ID: 4726 | NADH:ubiquinone oxidoreductase subunit S6 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (1801407..1816048) | CI-13kA, CI-13kD-A, CI13KDA, MC1DN9 | 603848 |
ID: 56181 | mitochondrial fission regulator 1 like [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (25819954..25832938) | FAM54B, HYST1888, MST116, MSTP116 | 620765 |
ID: 84503 | zinc finger protein 527 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (37371099..37393066) | | |
ID: 79913 | actin related protein 5 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38748460..38772520) | Arp5, INO80M | 619730 |
ID: 9025 | ring finger protein 8 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (37353983..37394734) | hRNF8 | 611685 |
ID: 348801 | leukemia NUP98 fusion partner 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (100401539..100456319) | NP3 | |
ID: 200942 | kelch domain containing 8B [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49171598..49176486) | CHL | 613169 |
ID: 54732 | transmembrane p24 trafficking protein 9 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (177592203..177597242) | GMP25, HSGP25L2G, p24a2, p24alpha2, p25 | 620436 |
ID: 60625 | DEAH-box helicase 35 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38962344..39039721) | C20orf15, DDX35, KAIA0875 | |