ID: 51025 | presequence translocase associated motor 16 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4340251..4351321, complement) | CGI-136, MAGMAS, SMDMDM, TIM16, TIMM16 | 614336 |
ID: 25920 | negative elongation factor complex member B [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (137255327..137273542) | COBRA1, NELF-B | 611180 |
ID: 51228 | glycolipid transfer protein [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109850945..109880541, complement) | | 608949 |
ID: 1847 | dual specificity phosphatase 5 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (110497907..110511533) | DUSP, HVH3 | 603069 |
ID: 64400 | AKT interacting protein [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (53491040..53504412, complement) | FT1, FTS | 608483 |
ID: 375743 | protein prenyltransferase alpha subunit repeat containing 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (69709525..69760011, complement) | | |
ID: 9416 | DEAD-box helicase 23 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48829756..48852163, complement) | PRPF28, SNRNP100, U5-100K, U5-100KD, prp28 | 612172 |
ID: 340371 | nuclear receptor binding protein 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (143829776..143840973, complement) | TRG16, pp9320 | 615563 |
ID: 55454 | chondroitin sulfate N-acetylgalactosaminyltransferase 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (43138445..43185308) | CHGN2, ChGn-2, GALNACT-2, GALNACT2, PRO0082, beta4GalNAcT | 616616 |
ID: 29894 | cleavage and polyadenylation specific factor 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144393231..144409335, complement) | CPSF160, HSU37012, MYP27, P/cl.18 | 606027 |
ID: 81631 | microtubule associated protein 1 light chain 3 beta [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87392336..87404774) | ATG8F, LC3B, MAP1A/1BLC3-a, MAP1LC3B | 609604 |
ID: 79174 | cysteine rich with EGF like domains 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (49918634..49927537) | | 607171 |
ID: 896 | cyclin D3 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (41934933..42050035, complement) | | 123834 |
ID: 90427 | Bcl2 modifying factor [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (40087890..40108879, complement) | | 606266 |
ID: 23268 | dynamin binding protein [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (99875571..100009947, complement) | ARHGEF36, CTRCT48, TUBA | 611282 |
ID: 55783 | cap methyltransferase 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71281392..71289722, complement) | AFT, FTSJD1, HMTr2, MTr2 | 616190 |
ID: 65998 | zinc finger translocation associated [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (63759892..63768775, complement) | C11orf95 | 615699 |