ID: 5147 | phosphodiesterase 6D [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (231732433..231781282, complement) | JBTS22, PDED | 602676 |
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: 335 | apolipoprotein A1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116835751..116837622, complement) | AMYLD3, HPALP2, apo(a) | 107680 |
ID: 387 | ras homolog family member A [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49359145..49411976, complement) | ARH12, ARHA, EDFAOB, RHO12, RHOH12 | 165390 |
ID: 4000 | lamin A/C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156082573..156140081) | CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL, FPLD, FPLD2, HGPS, IDC, LDP1, LFP, LGMD1B, LMN1, LMNC, LMNL1, MADA, PRO1 | 150330 |
ID: 5265 | serpin family A member 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (94376747..94390635, complement) | A1A, A1AT, AAT, PI, PI1, PRO2275, alpha1AT, nNIF | 107400 |
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: 213 | albumin [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73404287..73421482) | FDAHT, HSA, PRO0883, PRO0903, PRO1341 | 103600 |
ID: 4089 | SMAD family member 4 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (51030213..51085042) | DPC4, JIP, MADH4, MYHRS | 600993 |
ID: 718 | complement C3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (6677704..6720650, complement) | AHUS5, ARMD9, ASPa, C3b, CPAMD1, HEL-S-62p, C3 | 120700 |
ID: 998 | cell division cycle 42 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (22052709..22101360) | CDC42Hs, G25K, TKS | 116952 |
ID: 3240 | haptoglobin [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (72054505..72061055) | BP2ALPHA2, HPA1S, HP | 140100 |
ID: 2244 | fibrinogen beta chain [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (154562980..154572807) | HEL-S-78p | 134830 |
ID: 7018 | transferrin [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (133661998..133796641) | HEL-S-71p, PRO1557, PRO2086QTL1, TF | 190000 |
ID: 2266 | fibrinogen gamma chain [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (154604136..154612656, complement) | | 134850 |
ID: 8454 | cullin 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (148697756..148801110) | | 603134 |
ID: 2 | alpha-2-macroglobulin [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (9067708..9116229, complement) | A2MD, CPAMD5, FWP007, S863-7 | 103950 |
ID: 6500 | S-phase kinase associated protein 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (134148935..134176950, complement) | EMC19, OCP-II, OCP2A, TCEB1L, p19A, SKP1 | 601434 |
ID: 6103 | retinitis pigmentosa GTPase regulator [Homo sapiens (human)] | Chromosome X, NC_000023.11 (38269163..38327509, complement) | COD1, CORDX1, CRD, PCDX, RP15, RP3, XLRP3, orf15 | 312610 |
ID: 12 | serpin family A member 3 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (94612391..94624053) | AACT, ACT, GIG24, GIG25 | 107280 |