ID: 63915 | biogenesis of lysosomal organelles complex 1 subunit 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (8013567..8064414, complement) | BLOS5, HPS11, MU, MUTED | 607289 |
ID: 351 | amyloid beta precursor protein [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (25880550..26171128, complement) | AAA, ABETA, ABPP, AD1I, CTFgamma, CVAP, PN-II, PN2, alpha-sAPP, preA4, APP | 104760 |
ID: 100526836 | BLOC1S5-TXNDC5 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (7881250..8064414, complement) | MUTED-TXNDC5 | |
ID: 100526837 | EEF1E1-BLOC1S5 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (8013567..8102595, complement) | EEF1E1-MUTED | |
ID: 8878 | sequestosome 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (179806393..179838078) | A170, DMRV, EBIAP, FTDALS3, NADGP, OSIL, PDB3, ZIP3, p60, p62, p62B | 601530 |
ID: 7514 | exportin 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (61477849..61538612, complement) | CRM-1, CRM1, emb, exp1 | 602559 |
ID: 84062 | dystrobrevin binding protein 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (15522807..15663058, complement) | BLOC1S8, DBND, HPS7, My031, SDY | 607145 |
ID: 10075 | HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (53532096..53686719, complement) | ARF-BP1, HECTH9, HSPC272, Ib772, LASU1, MRXST, MULE, URE-B1, UREB1 | 300697 |
ID: 1454 | casein kinase 1 epsilon [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38290691..38318084, complement) | CKIe, CKIepsilon, HCKIE | 600863 |
ID: 6710 | spectrin beta, erythrocytic [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64746283..64879907, complement) | EL3, HS2, HSPTB1, SPH2 | 182870 |
ID: 81567 | thioredoxin domain containing 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (7881517..7910788, complement) | ENDOPDI, ERP46, HCC-2, HCC2, PDIA15, STRF8, UNQ364 | 616412 |
ID: 6273 | S100 calcium binding protein A2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (153561108..153565844, complement) | CAN19, S100L | 176993 |
ID: 8338 | H2A clustered histone 20 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (149886918..149887411) | H2A, H2A-GL101, H2A/q, H2AFQ, HIST2H2AC | 602797 |
ID: 8991 | selenium binding protein 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151364304..151372705, complement) | EHMTO, HEL-S-134P, LPSB, MTO, SBP56, SP56, hSBP | 604188 |
ID: 3009 | H1.5 linker histone, cluster member [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (27866792..27867588, complement) | H1, H1.5, H1B, H1F5, H1s-3, HIST1H1B | 142711 |
ID: 6602 | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50085342..50100707) | BAF60A, CRACD1, CSS11, Rsc6p | 601735 |
ID: 9342 | synaptosome associated protein 29 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (20859007..20891214) | CEDNIK, SNAP-29 | 604202 |
ID: 11339 | Opa interacting protein 5 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (41309273..41332591, complement) | 5730547N13Rik, CT86, LINT-25, MIS18B, MIS18beta, hMIS18beta | 606020 |
ID: 54165 | defective in cullin neddylation 1 domain containing 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182938074..182985918, complement) | DCNL1, DCUN1L1, RP42, SCCRO, SCRO, Tes3 | 605905 |
ID: 9521 | eukaryotic translation elongation factor 1 epsilon 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (8073360..8102548, complement) | AIMP3, P18 | 609206 |