ID: 7353 | ubiquitin recognition factor in ER associated degradation 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19449911..19479193, complement) | UFD1L | 601754 |
ID: 6605 | SWI/SNF related BAF chromatin remodeling complex subunit E1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (40624962..40647818, complement) | BAF57, CSS5 | 603111 |
ID: 2597 | glyceraldehyde-3-phosphate dehydrogenase [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (6534517..6538371) | G3PD, GAPD, HEL-S-162eP | 138400 |
ID: 8503 | phosphoinositide-3-kinase regulatory subunit 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (46040140..46174901, complement) | p55, p55-GAMMA, p55PIK | 606076 |
ID: 5511 | protein phosphatase 1 regulatory subunit 8 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (27830782..27851676) | ARD-1, ARD1, NIPP-1, NIPP1, PRO2047 | 602636 |
ID: 30000 | transportin 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12699201..12723932, complement) | IDDHISD, IPO3, KPNB2B, TRN2 | 603002 |
ID: 25870 | sulfatase modifying factor 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (56064286..56087946) | pFGE | 607940 |
ID: 79637 | armadillo repeat containing 7 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (75109969..75130272) | | |
ID: 10069 | RWD domain containing 2B [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (29004384..29019349, complement) | C21orf6, GL011 | 617843 |
ID: 3981 | DNA ligase 4 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (108207442..108218349, complement) | LIG4S | 601837 |
ID: 84945 | abhydrolase domain containing 13 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (108218392..108234243) | BEM46L1, C13orf6, bA153I24.2 | |
ID: 81857 | mediator complex subunit 25 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49818289..49840384) | ACID1, ARC92, BVSYS, CMT2B2, P78, PTOV2, TCBAP0758 | 610197 |
ID: 22882 | zinc fingers and homeoboxes 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (122780379..122974510) | AFR1, RAF | 609185 |
ID: 751071 | citrate synthase lysine methyltransferase [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (62665312..62668108) | CS-KMT, METTL12, U99HG | 617897 |
ID: 90576 | zinc finger protein 799 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12390016..12415084, complement) | HIT-40, HIT40, ZNF842 | 619916 |
ID: 81853 | transmembrane protein 14B [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (10747759..10759774) | | 619865 |
ID: 80789 | integrator complex subunit 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (62646848..62653302, complement) | INT5, KIAA1698 | 611349 |
ID: 5826 | ATP binding cassette subfamily D member 4 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74285269..74302934, complement) | ABC41, EST352188, MAHCJ, P70R, P79R, PMP69, PXMP1L | 603214 |
ID: 50999 | transmembrane p24 trafficking protein 5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (93149742..93180413, complement) | CGI-100, p24g2, p28 | 616876 |
ID: 5451 | POU class 2 homeobox 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (167220885..167427345) | OCT1, OTF1, Oct1Z, oct-1B | 164175 |