ID: 136371 | ankyrin repeat and SOCS box containing 10 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (151175698..151187792, complement) | GLC1F | 615054 |
ID: 3934 | lipocalin 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128149453..128153453) | 24p3, MSFI, NGAL, p25 | 600181 |
ID: 7316 | ubiquitin C [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (124911646..124914650, complement) | HMG20 | 191340 |
ID: 3315 | heat shock protein family B (small) member 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (76302673..76304292) | CMT2F, HEL-S-102, HMN2B, HMND3, HS.76067, HSP27, HSP28, Hsp25, SRP27 | 602195 |
ID: 3303 | heat shock protein family A (Hsp70) member 1A [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31815543..31817942) | HEL-S-103, HSP70, HSP70-1, HSP70-1A, HSP70-2, HSP70.1, HSP70.2, HSP70I, HSP72, HSPA1 | 140550 |
ID: 23028 | lysine demethylase 1A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23019468..23083689) | AOF2, BHC110, CPRF, KDM1, LSD1 | 609132 |
ID: 10273 | STIP1 homology and U-box containing protein 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (680410..682801) | CHIP, HSPABP2, NY-CO-7, SCA48, SCAR16, SDCCAG7, UBOX1 | 607207 |
ID: 2010 | emerin [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154379295..154381523) | EDMD, LEMD5, STA | 300384 |
ID: 6921 | elongin C [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (73945119..73972287, complement) | SIII, TCEB1 | 600788 |
ID: 8065 | cullin 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (108008898..108107761) | CUL-5, VACM-1, VACM1 | 601741 |
ID: 6923 | elongin B [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2771414..2777280, complement) | SIII, TCEB2 | 600787 |
ID: 1917 | eukaryotic translation elongation factor 1 alpha 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63488014..63499083, complement) | DEE33, EEF1AL, EF-1-alpha-2, EF1A, EIEE33, HS1, MRD38, STN, STNL | 602959 |
ID: 292 | solute carrier family 25 member 5 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (119468444..119471396) | 2F1, AAC2, ANT2, T2, T3 | 300150 |
ID: 55662 | hypoxia inducible factor 1 subunit alpha inhibitor [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (100535943..100559998) | FIH1 | 606615 |
ID: 7284 | Tu translation elongation factor, mitochondrial [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (28842411..28846348, complement) | COXPD4, EF-TuMT, EFTU, P43 | 602389 |
ID: 84168 | ANTXR cell adhesion molecule 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (69013144..69249327) | ATR, GAPO, TEM8 | 606410 |
ID: 192111 | PGAM family member 5, mitochondrial serine/threonine protein phosphatase [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (132710842..132722734) | BXLBV68 | 614939 |
ID: 6576 | solute carrier family 25 member 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19175581..19178736, complement) | CIC, CMS23, CTP, D2L2AD, SEA, SLC20A3 | 190315 |
ID: 5685 | proteasome 20S subunit alpha 4 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (78540405..78552417) | HC9, HsT17706, PSC9 | 176846 |
ID: 5250 | solute carrier family 25 member 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98593686..98606367) | OK/SW-cl.48, PHC, PTP, PiC | 600370 |