ID: 8635 | ribonuclease T2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (166922113..166956550, complement) | RNASE6PL, bA514O12.3 | 612944 |
ID: 57486 | neurolysin [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (65722205..65829283) | AGTBP, EP24.16, MEP, MOP | 611530 |
ID: 55614 | kinesin family member 16B [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (16272104..16573448, complement) | C20orf23, KISC20ORF, SNX23 | 618171 |
ID: 80233 | FA core complex associated protein 100 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (81539891..81553133, complement) | C17orf70 | 611301 |
ID: 283219 | potassium channel tetramerization domain containing 21 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (78171249..78188626, complement) | KCASH2 | 618790 |
ID: 66005 | chitinase domain containing 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (867859..915214, complement) | GL008, SI-CLP, SICLP | 615692 |
ID: 22887 | forkhead box J3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (42176548..42335880, complement) | | 616035 |
ID: 54677 | carnitine O-octanoyltransferase [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (87345664..87399794) | COT | 606090 |
ID: 85359 | DiGeorge syndrome critical region gene 6 like [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (20314238..20320060, complement) | DGCR6 | 609459 |
ID: 29960 | mitochondrial rRNA methyltransferase 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (2234195..2242205, complement) | FJH1, FTSJ2, HEL97, MTDPS17, RRMJ2 | 606906 |
ID: 112611 | RWD domain containing 2A [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (83193357..83198935) | RWDD2, dJ747H23.2 | |
ID: 201292 | tripartite motif containing 65 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (75879537..75896951, complement) | 4732463G12Rik | 619408 |
ID: 889 | KRIT1 ankyrin repeat containing [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (92198969..92246100, complement) | CAM, CCM1 | 604214 |
ID: 54557 | small glutamine rich tetratricopeptide repeat co-chaperone beta [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (65665928..65723013, complement) | SGT2 | 620526 |
ID: 388962 | bolA family member 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (74135400..74147912, complement) | MMDS2 | 613183 |
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: 4521 | nudix hydrolase 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (2242226..2251145) | MTH1 | 600312 |
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: 55113 | XK related 8 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (27959973..27968093) | XRG8, hXkr8 | 619940 |
ID: 8723 | sorting nexin 4 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (125446650..125520202, complement) | ATG24B | 605931 |