ID: 3713 | involucrin [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (152908546..152911886) | | 147360 |
ID: 107880064 | IVL promoter region [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (152906047..152909786) | | |
ID: 999 | cadherin 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (68737292..68835537) | Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM, UVO | 192090 |
ID: 6794 | serine/threonine kinase 11 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (1205778..1228431) | LKB1, PJS, hLKB1 | 602216 |
ID: 65018 | PTEN induced kinase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (20633458..20651511) | BRPK, PARK6 | 608309 |
ID: 252995 | fibronectin type III domain containing 5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (32862268..32872484, complement) | FRCP2, irisin | 611906 |
ID: 3312 | heat shock protein family A (Hsp70) member 8 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (123057489..123062462, complement) | HEL-33, HEL-S-72p, HSC54, HSC70, HSC71, HSP71, HSP73, HSPA10, LAP-1, LAP1, NIP71 | 600816 |
ID: 1509 | cathepsin D [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (1752755..1763927, complement) | CLN10, CPSD, HEL-S-130P | 116840 |
ID: 51741 | WW domain containing oxidoreductase [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (78099654..79212667) | D16S432E, DEE28, EIEE28, FOR, FRA16D, HHCMA56, PRO0128, SCAR12, SDR41C1, WOX1 | 605131 |
ID: 3178 | heterogeneous nuclear ribonucleoprotein A1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (54280726..54287087) | ALS19, ALS20, HNRPA1, HNRPA1L3, IBMPFD3, MPD3, UP 1, hnRNP A1, hnRNP-A1 | 164017 |
ID: 4878 | natriuretic peptide A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (11845709..11847783, complement) | ANF, ANP, ATFB6, ATRST2, CDD, CDD-ANF, CDP, PND | 108780 |
ID: 5268 | serpin family B member 5 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (63476958..63505085) | PI5, maspin | 154790 |
ID: 10892 | MALT1 paracaspase [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (58671465..58754477) | IMD12, MLT, MLT1, PCASP1 | 604860 |
ID: 6737 | tripartite motif containing 21 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (4384897..4393702, complement) | RNF81, RO52, Ro/SSA, SSA, SSA1 | 109092 |
ID: 2177 | FA complementation group D2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (10026437..10101932) | FA-D2, FA4, FACD, FAD, FAD2, FANCD | 613984 |
ID: 59 | actin alpha 2, smooth muscle [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (88935074..88991337, complement) | ACTSA, SMDYS | 102620 |
ID: 1832 | desmoplakin [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (7541671..7586714) | DCWHKTA, DP | 125647 |
ID: 2810 | stratifin [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (26863149..26864456) | YWHAS | 601290 |
ID: 1398 | CRK proto-oncogene, adaptor protein [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (1420693..1456232, complement) | CRKII, p38 | 164762 |
ID: 2495 | ferritin heavy chain 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (61964285..61967634, complement) | FHC, FTH, FTHL6, HFE5, NBIA9, PIG15, PLIF | 134770 |