ID: 54760 | proprotein convertase subtilisin/kexin type 4 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (1481428..1490876, complement) | PC4, SPC5 | 600487 |
ID: 25903 | olfactomedin like 2B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (161983192..162023869, complement) | | |
ID: 56648 | eukaryotic translation initiation factor 5A2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (170888418..170908637, complement) | EIF-5A2, eIF5AII | 605782 |
ID: 9997 | synthesis of cytochrome C oxidase 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (50523568..50526442, complement) | CEMCOX1, ECGF1, Gliostatin, MC4DN2, MYP6, PD-ECGF, SCO1L, TP, TYMP, TdRPase | 604272 |
ID: 55721 | IQ motif containing C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (32205671..32208682) | | |
ID: 5351 | procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (11934717..11975537) | EDS6, EDSKCL1, LH, LH1, LLH, PLOD | 153454 |
ID: 440307 | tubulin tyrosine ligase like 13 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (90249556..90265477) | TTLL13P | 620485 |
ID: 84929 | fibrinogen C domain containing 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (130902440..130940709, complement) | | 613357 |
ID: 10535 | ribonuclease H2 subunit A [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12806584..12813640) | AGS4, JUNB, RNASEHI, RNHIA, RNHL | 606034 |
ID: 126295 | zinc finger protein 57 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2900928..2918473) | ZNF424 | |
ID: 51663 | zinc finger RNA binding protein [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (32354350..32444740, complement) | SPG711, ZFR | 615635 |
ID: 79734 | potassium channel tetramerization domain containing 17 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37051742..37063390) | | 616386 |
ID: 3690 | integrin subunit beta 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (47253827..47313743) | BDPLT16, BDPLT2, BDPLT24, CD61, GP3A, GPIIIa, GT, GT2 | 173470 |
ID: 130399 | activin A receptor type 1C [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (157526767..157628864, complement) | ACVRLK7, ALK7 | 608981 |
ID: 2827 | G protein-coupled receptor 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (27392622..27395814) | ACCA | 600241 |
ID: 56474 | CTP synthase 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (16587999..16712910, complement) | GATD5B | 300380 |
ID: 6510 | solute carrier family 1 member 5 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46774883..46788594, complement) | AAAT, ASCT2, ATBO, M7V1, M7VS1, R16, RDRC | 109190 |
ID: 55036 | coiled-coil domain 40 molecular ruler complex subunit [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80036642..80100613) | CFAP172, CILD15, FAP172 | 613799 |
ID: 26577 | procollagen C-endopeptidase enhancer 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (142817874..142889083, complement) | PCPE2 | 607064 |
ID: 286151 | F-box protein 43 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (100133351..100150569, complement) | EMI2, ERP1, FBX43, OOMD12, OZEMA12, SPGF64 | 609110 |