ID: 8029 | cubilin [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (16823966..17129811, complement) | IFCR, IGS, IGS1, MGA1, gp280 | 602997 |
ID: 672 | BRCA1 DNA repair associated [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43044295..43170327, complement) | BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4, PPP1R53, PSCP, RNF53 | 113705 |
ID: 4318 | matrix metallopeptidase 9 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (46008908..46016561) | CLG4B, GELB, MANDP2, MMP-9 | 120361 |
ID: 7421 | vitamin D receptor [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (47841537..47904994, complement) | NR1I1, PPP1R163 | 601769 |
ID: 3958 | galectin 3 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (55129252..55145430) | CBP35, GAL3, GALBP, GALIG, L31, LGALS2, MAC2 | 153619 |
ID: 213 | albumin [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73404287..73421482) | FDAHT, HSA, PRO0883, PRO0903, PRO1341 | 103600 |
ID: 6927 | HNF1 homeobox A [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (120978543..121002512) | HNF-1-alpha, HNF-1A, HNF1, HNF1alpha, HNF4A, IDDM20, LFB1, MODY3, TCF-1, TCF1 | 142410 |
ID: 2638 | GC vitamin D binding protein [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (71741693..71805520, complement) | DBP, DBP-maf, DBP/GC, GRD3, Gc-MAF, GcMAF, HEL-S-51, VDB, VDBG, VDBP | 139200 |
ID: 867 | Cbl proto-oncogene [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (119206339..119308149) | C-CBL2, FRA11B, NSLL, RNF55, CBL | 165360 |
ID: 4035 | LDL receptor related protein 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (57128483..57213361) | A2MR, APOER, APR, CD91, DDH3, IGFBP-3R, IGFBP3R, IGFBP3R1, KPA, LRPA, TGFBR5, LRP1 | 107770 |
ID: 7018 | transferrin [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (133661998..133796641) | HEL-S-71p, PRO1557, PRO2086QTL1, TF | 190000 |
ID: 3990 | lipase C, hepatic type [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (58431991..58569844) | HDLCQ12, HL, HTGL, LIPH | 151670 |
ID: 6251 | Ras suppressor protein 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (16590611..16817424, complement) | RSP-1 | 179555 |
ID: 7356 | secretoglobin family 1A member 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (62419033..62423195) | CC10, CC16, CCPBP, CCSP, UGB, UP-1, UP1 | 192020 |
ID: 4036 | LDL receptor related protein 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (169127109..169362534, complement) | DBS, GP330, LRP-2 | 600073 |
ID: 3028 | hydroxysteroid 17-beta dehydrogenase 10 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (53431258..53434376, complement) | 17b-HSD10, ABAD, CAMR, DUPXp11.22, ERAB, HADH2, HCD2, HSD10MD, MHBD, MRPP2, MRX17, MRX31, MRXS10, SCHAD, SDR5C1 | 300256 |
ID: 23076 | ribosomal RNA processing 1B [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43659560..43696079) | KIAA0179, NNP1L, Nnp1, PPP1R136, RRP1 | 610654 |
ID: 10529 | nebulette [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (20779973..21293050, complement) | C10orf113, LASP2, LNEBL, bA165O3.1 | 605491 |
ID: 2694 | cobalamin binding intrinsic factor [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (59829273..59845499, complement) | GIF, IF, IFMH, INF, TCN3 | 609342 |
ID: 55022 | phosphotyrosine interaction domain containing 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (229023973..229271287, complement) | HMFN2073, NYGGF4, P-CLI1, PCLI1 | 612930 |