ID: 316 | aldehyde oxidase 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (200586014..200682241) | AO, AOH1 | 602841 |
ID: 729440 | coiled-coil domain containing 61 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45995467..46018616) | VFL3, hVFL3 | 620676 |
ID: 29097 | cornichon family member 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (224356803..224379452) | CNIH-4, CNIH2, HSPC163 | 617483 |
ID: 81890 | queuine tRNA-ribosyltransferase catalytic subunit 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10701439..10713365) | FP3235, TGT, TGUT | 609615 |
ID: 81608 | factor interacting with PAPOLA and CPSF1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (53377641..53460862) | FIP1, Rhe, hFip1 | 607686 |
ID: 11162 | nudix hydrolase 6 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (122892577..122922968, complement) | ASFGF2, FGF-AS, FGF2AS, GFG-1, GFG1 | 606261 |
ID: 80723 | solute carrier family 35 member G2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (136819126..136855888) | TMEM22 | 617812 |
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: 51566 | armadillo repeat containing X-linked 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (101623151..101627843) | ALEX3, GASP6, dJ545K15.2 | 300364 |
ID: 905 | cyclin T2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (134918822..134959342) | CYCT2 | 603862 |
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 |
ID: 168374 | zinc finger protein 92 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (65373855..65401136) | HEL-203, HPF12, HTF12, TF12 | 603974 |
ID: 55845 | BRICK1 subunit of SCAR/WAVE actin nucleating complex [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (10115675..10127190) | C3orf10, HSPC300, MDS027, hHBrk1 | 611183 |
ID: 5921 | RAS p21 protein activator 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (87267883..87391916) | CM-AVM, CMAVM, CMAVM1, GAP, PKWS, RASA, RASGAP, p120, p120GAP, p120RASGAP | 139150 |
ID: 28974 | chromosome 19 open reading frame 53 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (13774456..13778773) | HSPC023, L10K, LYDG10 | 620685 |
ID: 64689 | golgi reassembly stacking protein 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (39096599..39107627, complement) | GOLPH5, GRASP65, P65 | 606867 |
ID: 582 | Bardet-Biedl syndrome 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66510635..66533598) | BBS2L2 | 209901 |
ID: 54732 | transmembrane p24 trafficking protein 9 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (177592203..177597242) | GMP25, HSGP25L2G, p24a2, p24alpha2, p25 | 620436 |
ID: 54872 | phosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (499210..540200) | EMM, GPI7, LAS21, MRT53, NEDHSCA, PRO4405, RLGS1930 | 616918 |
ID: 55973 | B cell receptor associated protein 29 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (107580007..107623317) | B29, BAP29 | 619612 |