ID: 7355 | solute carrier family 35 member A2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (48903183..48911958, complement) | CDG2M, CDGX, UDP-Gal-Tr, UGALT, UGAT, UGT, UGT1, UGT2, UGTL | 314375 |
ID: 3845 | KRAS proto-oncogene, GTPase [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (25205246..25250929, complement) | 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A, K-RAS4B, K-Ras, K-Ras 2, KI-RAS1, KRAS2, NS, NS3, OES, RALD, RASK2, c-Ki-ras, c-Ki-ras2, KRAS | 190070 |
ID: 5621 | prion protein (Kanno blood group) [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (4686456..4701588) | ASCR, AltPrP, CD230, CJD, GSS, KURU, PRIP, PrP, PrP27-30, PrP33-35C, PrPc, p27-30 | 176640 |
ID: 3265 | HRas proto-oncogene, GTPase [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (532242..535576, complement) | C-BAS/HAS, C-H-RAS, C-HA-RAS1, CTLO, H-RASIDX, HAMSV1, RASH1, p21ras, HRAS | 190020 |
ID: 328 | apurinic/apyrimidinic endodeoxyribonuclease 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20455226..20457767) | APE, APE1, APEN, APEX, APX, HAP1, REF1 | 107748 |
ID: 4893 | NRAS proto-oncogene, GTPase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (114704469..114716771, complement) | ALPS4, CMNS, KRAS, N-ras, NCMS1, NS6, NRAS | 164790 |
ID: 768 | carbonic anhydrase 9 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35673928..35681159) | CAIX, MN | 603179 |
ID: 2194 | fatty acid synthase [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (82078338..82098236, complement) | FAS, OA-519, SDR27X1 | 600212 |
ID: 4162 | melanoma cell adhesion molecule [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (119308529..119317130, complement) | CD146, HEMCAM, METCAM, MUC18, MelCAM | 155735 |
ID: 7879 | RAB7A, member RAS oncogene family [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (128726183..128814798) | CMT2B, PRO2706, RAB7 | 602298 |
ID: 5336 | phospholipase C gamma 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (81739041..81962685) | APLAID, FCAS3, PLC-IV, PLC-gamma-2 | 600220 |
ID: 5359 | phospholipid scramblase 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (146515180..146544607, complement) | MMTRA1B | 604170 |
ID: 4249 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134119935..134454621) | GNT-V, GNT-VAA, glcNAc-T V, MGAT5 | 601774 |
ID: 5645 | serine protease 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (142770970..142774560) | TRY2, TRY8, TRYP2 | 601564 |
ID: 5862 | RAB2A, member RAS oncogene family [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (60516910..60623644) | LHX, RAB2 | 179509 |
ID: 1295 | collagen type VIII alpha 1 chain [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (99638594..99799217) | C3orf7 | 120251 |
ID: 60481 | ELOVL fatty acid elongase 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (53267404..53348950, complement) | HELO1, SCA38, dJ483K16.1 | 611805 |
ID: 4245 | alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (180784780..180815616, complement) | GLCNAC-TI, GLCT1, GLYT1, GNT-1, GNT-I, GnTI, MGAT | 160995 |
ID: 8940 | DNA topoisomerase III beta [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21957025..21982787, complement) | TOP3B1 | 603582 |
ID: 10559 | solute carrier family 35 member A1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (87472974..87512336) | CDG2F, CMPST, CST, hCST | 605634 |