ID: 114991 | zinc finger protein 618 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (113876309..114056593) | FP13169, NEDD10 | 617077 |
ID: 158405 | KIAA1958 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (112486827..112669397) | | 617390 |
ID: 30837 | suppressor of cytokine signaling 7 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (38351844..38405593) | NAP4, NCKAP4 | 608788 |
ID: 9722 | nitric oxide synthase 1 adaptor protein [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (162069691..162370475) | 6330408P19Rik, CAPON, NPHS22 | 605551 |
ID: 648 | BMI1 proto-oncogene, polycomb ring finger [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (22321099..22331706) | FLVI2/BMI1, PCGF4, RNF51, flvi-2/bmi-1 | 164831 |
ID: 115207 | potassium channel tetramerization domain containing 12 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (76880175..76886405, complement) | C13orf2, PFET1, PFETIN | 610521 |
ID: 55700 | MAP7 domain containing 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36156160..36180849) | PARCC1, RPRC1 | |
ID: 200845 | potassium channel tetramerization domain containing 6 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (58492096..58502360) | KCASH3 | 618791 |
ID: 56950 | SET and MYND domain containing 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (214281159..214337131) | HSKM-B, KMT3C, ZMYND14 | 610663 |
ID: 7468 | nuclear receptor binding SET domain protein 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (1871393..1982192) | KMT3F, KMT3G, MMSET, RAUST, REIIBP, TRX5, WHS, WHSC1 | 602952 |
ID: 3069 | high density lipoprotein binding protein [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241227291..241315672, complement) | HBP, PRO2900, VGL | 142695 |
ID: 27347 | serine/threonine kinase 39 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (167954022..168247595, complement) | DCHT, PASK, SPAK | 607648 |
ID: 6150 | mitochondrial ribosomal protein L23 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (1947332..2014944) | L23MRP, RPL23, RPL23L, uL23m | 600789 |
ID: 8295 | transformation/transcription domain associated protein [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (98878532..99013241) | DEDDFA, DFNA75, PAF350/400, PAF400, STAF40, TR-AP, Tra1 | 603015 |
ID: 81846 | SET binding factor 2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (9778668..10304841, complement) | CMT4B2, DENND7B, MTMR13 | 607697 |
ID: 112398 | egl-9 family hypoxia inducible factor 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40799191..40808434) | EIT-6, EIT6, HIF-PH1, HIFPH1, HPH-1, HPH-3, PHD1 | 606424 |
ID: 161436 | EMAP like 5 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (88612431..88792953, complement) | EMAP-2, EMAP-5, FAP16 | 618119 |
ID: 1789 | DNA methyltransferase 3 beta [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (32762385..32809356) | FSHD4, ICF, ICF1, M.HsaIIIB | 602900 |
ID: 23648 | single stranded DNA binding protein 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (54225432..54413490, complement) | CSDP, SSDP, SSDP1 | 607390 |
ID: 6576 | solute carrier family 25 member 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19175581..19178736, complement) | CIC, CMS23, CTP, D2L2AD, SEA, SLC20A3 | 190315 |