ID: 29960 | mitochondrial rRNA methyltransferase 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (2234195..2242205, complement) | FJH1, FTSJ2, HEL97, MTDPS17, RRMJ2 | 606906 |
ID: 4521 | nudix hydrolase 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (2242226..2251145) | MTH1 | 600312 |
ID: 150678 | COP9 signalosome subunit 9 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (240126548..240136347, complement) | CSNAP, MYEOV2 | 619349 |
ID: 8379 | mitotic arrest deficient 1 like 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (1815795..2232945, complement) | MAD1, MVA7, PIG9, TP53I9, TXBP181 | 602686 |
ID: 81554 | RCC1 like [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (75027119..75073802, complement) | WBSCR16 | 620739 |
ID: 84612 | par-6 family cell polarity regulator beta [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50731580..50753741) | PAR6B | 608975 |
ID: 8723 | sorting nexin 4 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (125446650..125520202, complement) | ATG24B | 605931 |
ID: 55275 | VPS53 subunit of GARP complex [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (508668..714839, complement) | HCCS1, PCH2E, hVps53L, pp13624 | 615850 |
ID: 1841 | deoxythymidylate kinase [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (241675747..241686815, complement) | CDC8, CONPM, PP3731, TMPK, TYMK | 188345 |
ID: 80025 | pantothenate kinase 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3888781..3929887) | C20orf48, HARP, HSS, NBIA1, PKAN | 606157 |
ID: 66005 | chitinase domain containing 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (867859..915214, complement) | GL008, SI-CLP, SICLP | 615692 |
ID: 125488 | tetratricopeptide repeat domain 39C [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (23992887..24135600) | C18orf17, HsT2697 | |
ID: 197342 | essential meiotic structure-specific endonuclease subunit 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1772810..1781702) | SLX2B, gs125 | 610886 |
ID: 64949 | mitochondrial ribosomal protein S26 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3046052..3048250) | C20orf193, GI008, MRP-S13, MRP-S26, MRPS13, NY-BR-87, RPMS13, dJ534B8.3, mS26 | 611988 |
ID: 92675 | D-aminoacyl-tRNA deacylase 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (18588054..18766644) | C20orf88, DTD, DUE-B, DUEB, HARS2, pqn-68 | 610996 |
ID: 22876 | inositol polyphosphate-5-phosphatase F [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (119726050..119829147) | MSTP007, MSTPO47, SAC2, hSAC2 | 609389 |
ID: 6888 | transaldolase 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (747464..765012) | TAL, TAL-H, TALDOR, TALH | 602063 |
ID: 26164 | mitochondrial ribosome associated GTPase 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (62183028..62203568) | GTPBP5, ObgH1, dJ1005F21.2 | 610919 |
ID: 55262 | trafficking protein particle complex subunit 14 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (100154423..100158723, complement) | C7orf43, MAP11, MCPH25 | 618350 |
ID: 85359 | DiGeorge syndrome critical region gene 6 like [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (20314238..20320060, complement) | DGCR6 | 609459 |