ID: 2649 | nuclear receptor subfamily 6 group A member 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (124517275..124771311, complement) | CT150, GCNF, GCNF1, NR61, RTR, hGCNF, hRTR | 602778 |
ID: 375743 | protein prenyltransferase alpha subunit repeat containing 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (69709525..69760011, complement) | | |
ID: 6341 | synthesis of cytochrome C oxidase 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (10672474..10697533, complement) | MC4DN4, SCOD1 | 603644 |
ID: 124402 | UBA like domain containing 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4608884..4614888, complement) | FAM100A, PP11303 | |
ID: 9377 | cytochrome c oxidase subunit 5A [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (74919791..74938073, complement) | COX, COX-VA, MC4DN20, VA | 603773 |
ID: 79641 | rogdi atypical leucine zipper [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4796968..4802633, complement) | KTZS, RAV2, ROGD1 | 614574 |
ID: 54925 | zinc finger and SCAN domain containing 32 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (3382085..3401004, complement) | HCCS-5, ZNF434 | |
ID: 124045 | spermatogenesis associated 33 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89657776..89670458) | C16orf55 | 615409 |
ID: 56985 | ADP-ribose/CDP-alcohol diphosphatase, manganese dependent [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (10697594..10711558) | C17orf48, MDS006, NBLA03831 | |
ID: 84937 | zinc and ring finger 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (74999024..75110994) | NIN283 | 612060 |
ID: 84933 | chromosome 8 open reading frame 76 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123219967..123241377, complement) | | |
ID: 23545 | ATPase H+ transporting V0 subunit a2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123712353..123761755) | A2, ARCL, ARCL2A, ATP6A2, ATP6N1D, J6B7, RTF, STV1, TJ6, TJ6M, TJ6S, VPH1, WSS, a2V | 611716 |
ID: 54542 | ring finger and CCCH-type domains 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (122844556..122905359, complement) | MNAB, RNF164 | 615231 |
ID: 5119 | charged multivesicular body protein 1A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89644435..89657708, complement) | CHMP1, PCH8, PCOLN3, PRSM1, VPS46-1, VPS46A | 164010 |
ID: 56890 | Mdm1 nuclear protein [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (68294566..68332362, complement) | | 613813 |
ID: 123263 | mitochondrial methionyl-tRNA formyltransferase [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (65001512..65029639, complement) | COXPD15, FMT1, MC1DN27 | 611766 |
ID: 51291 | GEM interacting protein [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (19629476..19643657, complement) | ARHGAP46 | 609694 |
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: 55072 | ring finger protein 31 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (24146875..24160655) | HOIP, IMD115, Paul, ZIBRA | 612487 |
ID: 310 | annexin A7 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (73375101..73414058, complement) | ANX7, SNX, SYNEXIN | 186360 |