ID: 9530 | BAG cochaperone 4 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (38176855..38213301) | BAG-4, SODD | 603884 |
ID: 27257 | LSM1 homolog, mRNA degradation associated [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (38163321..38176730, complement) | CASM, YJL124C | 607281 |
ID: 6156 | ribosomal protein L30 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98041721..98045545, complement) | L30, eL30 | 180467 |
ID: 10598 | activator of HSP90 ATPase activity 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (77457867..77469472) | AHA1, C14orf3, hAha1, p38 | 608466 |
ID: 3839 | karyopherin subunit alpha 3 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (49699320..49792682, complement) | IPOA4, SPG88, SRP1, SRP1gamma, SRP4, hSRP1 | 601892 |
ID: 64081 | phenazine biosynthesis like protein domain containing [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (68282660..68332928, complement) | HEL-S-306, MAWBP, MAWDBP | 612189 |
ID: 24138 | interferon induced protein with tetratricopeptide repeats 5 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (89414568..89420997) | ISG58, P58, RI58 | 616135 |
ID: 1317 | solute carrier family 31 member 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (113221544..113264492) | COPT1, CTR1, NSCT | 603085 |
ID: 26276 | VPS33B late endosome and lysosome associated [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (90998416..91022621, complement) | KDIDAR, PFIC12 | 608552 |
ID: 51026 | golgi transport 1B [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (21501789..21518408) | CGI-141, GCT2, GOT1, GOT1B, YMR292W | 615078 |
ID: 26589 | mitochondrial ribosomal protein L46 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (88459478..88467388, complement) | C15orf4, LIECG2, P2ECSL, mL46 | 611851 |
ID: 3190 | heterogeneous nuclear ribonucleoprotein K [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83968083..83980615, complement) | AUKS, CSBP, HNRPK, TUNP | 600712 |
ID: 84268 | RPA interacting protein [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (5420182..5432877) | HRIP, RIP | 617299 |
ID: 10558 | serine palmitoyltransferase long chain base subunit 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (92031147..92115413, complement) | ALS27, HSAN1, HSN1, LBC1, LCB1, SPT1, SPTI | 605712 |
ID: 9847 | C2 calcium dependent domain containing 5 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (22448583..22544542, complement) | CDP138, KIAA0528 | 618044 |
ID: 55833 | ubiquitin associated protein 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (33921693..34049199, complement) | UBAP-2 | |
ID: 55151 | transmembrane protein 38B [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (105694541..105776629) | C9orf87, D4Ertd89e, OI14, TRIC-B, TRICB, bA219P18.1 | 611236 |
ID: 57209 | zinc finger protein 248 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (37758538..37858103, complement) | bA162G10.3 | |
ID: 116224 | PP2A Aalpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (68780065..68785566) | C9orf42, FAM122A | 617249 |
ID: 10428 | craniofacial development protein 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (75293710..75433503, complement) | BCNT, BUCENTAUR, CENP-29, CP27, SWC5, Yeti, p97 | 608108 |