ID: 51809 | polypeptide N-acetylgalactosaminyltransferase 7 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (173168811..173323967) | GALNAC-T7, GalNAcT7 | 605005 |
ID: 117248 | polypeptide N-acetylgalactosaminyltransferase 15 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (16174680..16248224) | GALNACT15, GALNT13, GALNT7, GALNTL2, PIH5, pp-GalNAc-T15 | 615131 |
ID: 101930370 | GALNT7 divergent transcript [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (173131933..173169652, complement) | | |
ID: 407040 | microRNA 34a [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (9151668..9151777, complement) | MIRN34A, miRNA34A, mir-34, mir-34a | 611172 |
ID: 3107 | major histocompatibility complex, class I, C [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31268749..31272092, complement) | D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1 | 142840 |
ID: 8600 | TNF superfamily member 11 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (42562736..42608013) | CD254, ODF, OPGL, OPTB2, RANKL, TNLG6B, TRANCE, hRANKL2, sOdf | 602642 |
ID: 7161 | tumor protein p73 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (3652516..3736201) | CILD47, P73 | 601990 |
ID: 3117 | major histocompatibility complex, class II, DQ alpha 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32637406..32655272) | CELIAC1, DQ-A1, DQA1, HLA-DQA*, HLA-DQB1, HLA-DQA1 | 146880 |
ID: 5156 | platelet derived growth factor receptor alpha [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (54229293..54298245) | CD140A, PDGFR-2, PDGFR2 | 173490 |
ID: 4311 | membrane metalloendopeptidase [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (155024202..155183729) | CALLA, CD10, CMT2T, NEP, SCA43, SFE | 120520 |
ID: 406996 | microRNA 214 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (172138798..172138907, complement) | MIRN214, miRNA214, mir-214 | 610721 |
ID: 5727 | patched 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95442980..95516971, complement) | BCNS, BCNS1, NBCCS, PTC, PTC1, PTCH | 601309 |
ID: 6548 | solute carrier family 9 member A1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (27098809..27155125, complement) | APNH, LIKNS, NHE-1, NHE1, PPP1R143 | 107310 |
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 |
ID: 2548 | alpha glucosidase [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80101581..80119881) | LYAG | 606800 |
ID: 6520 | solute carrier family 3 member 2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (62856109..62888860) | 4F2, 4F2HC, 4T2HC, CD98, CD98HC, MDU1, NACAE | 158070 |
ID: 407042 | microRNA 34c [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (111513439..111513515) | MIRN34C, miRNA34C, mir-34c | 611375 |
ID: 3191 | heterogeneous nuclear ribonucleoprotein L [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (38836370..38852347, complement) | HNRPL, P/OKcl.14, hnRNP-L | 603083 |
ID: 5360 | phospholipid transfer protein [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45898620..45912155, complement) | BPIFE, HDLCQ9 | 172425 |