ID: 2590 | polypeptide N-acetylgalactosaminyltransferase 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230057789..230282122) | CDG2T, GalNAc-T2 | 602274 |
ID: 1956 | epidermal growth factor receptor [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (55019017..55211628) | ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS, PIG61, mENA | 131550 |
ID: 348 | apolipoprotein E [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (44905796..44909393) | AD2, APO-E, ApoE4, LDLCQ5, LPG | 107741 |
ID: 59272 | angiotensin converting enzyme 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (15518197..15607211, complement) | ACEH | 300335 |
ID: 3077 | homeostatic iron regulator [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (26087429..26098343) | HFE1, HH, HLA-H, MVCD7, TFQTL2 | 613609 |
ID: 4582 | mucin 1, cell surface associated [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155185824..155192915, complement) | ADMCKD, ADMCKD1, ADTKD2, CA 15-3, CD227, Ca15-3, EMA, H23AG, KL-6, MAM6, MCD, MCKD, MCKD1, MUC-1, MUC-1/SEC, MUC-1/X/ZD, PEM, PEMT, PUM, MUC1 | 158340 |
ID: 64127 | nucleotide binding oligomerization domain containing 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (50693606..50733075) | ACUG, BLAU, BLAUS, CARD15, CD, CLR16.3, IBD1, NLRC2B, PSORAS1, YAOS, NOD2 | 605956 |
ID: 255738 | proprotein convertase subtilisin/kexin type 9 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (55039548..55064852) | FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1, PC9 | 607786 |
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: 1071 | cholesteryl ester transfer protein [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (56961950..56983845) | BPIFF, HDLCQ10 | 118470 |
ID: 998 | cell division cycle 42 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (22052709..22101360) | CDC42Hs, G25K, TKS | 116952 |
ID: 5156 | platelet derived growth factor receptor alpha [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (54229293..54298245) | CD140A, PDGFR-2, PDGFR2 | 173490 |
ID: 116519 | apolipoprotein A5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (116789367..116792420, complement) | APOAV, RAP3 | 606368 |
ID: 5770 | protein tyrosine phosphatase non-receptor type 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50510383..50585241) | PTP1B | 176885 |
ID: 5727 | patched 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95442980..95516971, complement) | BCNS, BCNS1, NBCCS, PTC, PTC1, PTCH | 601309 |
ID: 6117 | replication protein A1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (1830005..1900082) | HSSB, MST075, PFBMFT6, REPA1, RF-A, RP-A, RPA70 | 179835 |
ID: 7416 | voltage dependent anion channel 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (133971871..134114540, complement) | PORIN, VDAC-1 | 604492 |
ID: 9636 | ISG15 ubiquitin like modifier [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (1013497..1014540) | G1P2, IFI15, IMD38, IP17, UCRP, hUCRP | 147571 |
ID: 4864 | NPC intracellular cholesterol transporter 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (23506184..23586506, complement) | NPC, POGZ, SLC65A1 | 607623 |
ID: 6348 | C-C motif chemokine ligand 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (36088256..36090143, complement) | G0S19-1, LD78, LD78ALPHA, MIP-1-alpha, MIP1A, SCI, SCYA3 | 182283 |