ID: 81502 | histocompatibility minor 13 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (31514442..31569543) | H13, IMP1, IMPAS, IMPAS-1, MSTP086, PSENL3, PSL3, SPP, SPPL1 | 607106 |
ID: 2547 | X-ray repair cross complementing 6 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41621295..41664041) | CTC75, CTCBF, G22P1, KU70, ML8, TLAA | 152690 |
ID: 7266 | DnaJ heat shock protein family (Hsp40) member C7 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41976435..42017439, complement) | DJ11, DJC7, TPR2, TTC2 | 601964 |
ID: 10527 | importin 7 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (9384652..9448127) | Imp7, RANBP7 | 605586 |
ID: 27300 | zinc finger protein 544 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (58228914..58277455) | | |
ID: 55300 | phosphatidylinositol 4-kinase type 2 beta [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (25234033..25279204) | PI4KIIB, PIK42B | 612101 |
ID: 79760 | gem nuclear organelle associated protein 7 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45075627..45091518) | SIP3 | 607419 |
ID: 64789 | exonuclease 5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (40508767..40516038) | C1orf176, DEM1, Exo V, hExo5 | 618601 |
ID: 254042 | methionyl aminopeptidase type 1D, mitochondrial [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (171999953..172082430) | MAP 1D, MAP1D, MetAP 1D, Metap1l | 610267 |
ID: 84335 | AKT1 substrate 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (49869033..49878356, complement) | Lobe, PRAS40 | 610221 |
ID: 285203 | EGF domain specific O-linked N-acetylglucosamine transferase [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (68975225..69013684, complement) | AER61, AOS4, C3orf641, EOGT | 614789 |
ID: 27010 | thiamin pyrophosphokinase 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (144451941..144836437, complement) | HTPK1, PP20, THMD5 | 606370 |
ID: 80854 | SET domain containing 7, histone lysine methyltransferase [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (139492974..139556219, complement) | KMT7, SET7, SET7/9, SET9 | 606594 |
ID: 81890 | queuine tRNA-ribosyltransferase catalytic subunit 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10701439..10713365) | FP3235, TGT, TGUT | 609615 |
ID: 738 | VPS51 subunit of GARP complex [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65096214..65111862) | ANG2, ANG3, C11orf2, C11orf3, FFR, PCH13 | 615738 |
ID: 79913 | actin related protein 5 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (38748460..38772520) | Arp5, INO80M | 619730 |
ID: 51204 | translational activator of cytochrome c oxidase I [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (63600895..63608365) | CCDC44, MC4DN8 | 612958 |
ID: 10943 | MSL complex subunit 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (11758159..11775772) | MRSXBA, MRXS36, MRXSBAL1, MSL3 | 300609 |
ID: 78987 | cysteine rich with EGF like domains 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (9933834..9945406) | AVSD2, CIRRIN, JELANS | 607170 |
ID: 1678 | translocase of inner mitochondrial membrane 8A [Homo sapiens (human)] | Chromosome X, NC_000023.11 (101345661..101348742, complement) | DDP, DDP1, DFN1, MTS, TIM8 | 300356 |