ID: 55343 | solute carrier family 35 member C1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (45804079..45813016) | CDG2C, FUCT1 | 605881 |
ID: 10401 | protein inhibitor of activated STAT 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (145848522..145859081, complement) | ZMIZ5 | 605987 |
ID: 57724 | ectopic P-granules 5 autophagy tethering factor [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (45800581..45967329, complement) | HEEW1, KIAA1632, VICIS | 615068 |
ID: 3927 | LIM and SH3 protein 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38870058..38921770) | Lasp-1, MLN50 | 602920 |
ID: 339448 | chromosome 1 open reading frame 174 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (3889133..3900272, complement) | | |
ID: 79084 | WD repeat domain 77 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (111439890..111449256, complement) | HKMT1069, MEP-50, MEP50, Nbla10071, p44, p44/Mep50 | 611734 |
ID: 79058 | ASPSCR1 tether for SLC2A4, UBX domain containing [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (81977629..82017406) | ASPCR1, ASPL, ASPS, RCC17, TUG, UBXD9, UBXN9 | 606236 |
ID: 55111 | pleckstrin homology domain containing J1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2229981..2236329, complement) | GNRPX | 617834 |
ID: 340481 | zinc finger DHHC-type palmitoyltransferase 21 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (14588797..14693432, complement) | DHHC-21, DHHC21, DNZ1, HSPC097 | 614605 |
ID: 113444 | small integral membrane protein 12 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (34850362..34859749, complement) | C1orf212 | |
ID: 9931 | helicase with zinc finger [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (67070444..67245989, complement) | DHRC, DRHC, HUMORF5 | 606699 |
ID: 64598 | motile sperm domain containing 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (100612162..100615377) | CDS3, NET30 | 609125 |
ID: 4201 | male-enhanced antigen 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (43011143..43016886, complement) | HYS, MEA | 143170 |
ID: 84299 | migration and invasion enhancer 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (39728510..39730532, complement) | C17orf37, C35, ORB3, RDX12, XTP4 | 611802 |
ID: 2309 | forkhead box O3 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (108559825..108684774) | AF6q21, FKHRL1, FKHRL1P2, FOXO2A, FOXO3 | 602681 |
ID: 4891 | solute carrier family 11 member 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50952263..51028886, complement) | AHMIO1, DCT1, DMT1, NRAMP2 | 600523 |
ID: 4729 | NADH:ubiquinone oxidoreductase core subunit V2 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (9102699..9134341) | CI-24k, MC1DN7 | 600532 |
ID: 23378 | ribosomal RNA processing 8 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (6595072..6603616, complement) | KIAA0409, NML | 615818 |
ID: 10482 | nuclear RNA export factor 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (62792130..62805440, complement) | MEX67, TAP | 602647 |
ID: 57719 | anoctamin 8 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17323223..17334855, complement) | KIAA1623, TMEM16H | 610216 |