ID: 9879 | DEAD-box helicase 46 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (134758779..134831121) | PRPF5, Prp5 | 617848 |
ID: 10322 | SMYD family member 5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (73214245..73227221) | NN8-4AG, RAI15, RRG1, ZMYND23 | 619114 |
ID: 29063 | zinc finger CCHC-type containing 4 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (25312774..25370383) | HSPC052, ZGRF4 | 611792 |
ID: 81608 | factor interacting with PAPOLA and CPSF1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (53377641..53460862) | FIP1, Rhe, hFip1 | 607686 |
ID: 54732 | transmembrane p24 trafficking protein 9 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (177592203..177597242) | GMP25, HSGP25L2G, p24a2, p24alpha2, p25 | 620436 |
ID: 57150 | small integral membrane protein 8 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (87322588..87342329) | C6orf162, dJ102H19.2 | |
ID: 52 | acid phosphatase 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (264947..278283) | HAAP, LMW-PTP, LMWPTP | 171500 |
ID: 345757 | family with sequence similarity 174 member A [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (100535374..100586741) | HGS_RE408, NS5ATP6, TMEM157, UNQ1912 | |
ID: 255520 | ELMO domain containing 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (140524168..140553770) | 9830169G11Rik | 610196 |
ID: 9648 | GRIP and coiled-coil domain containing 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (108449206..108509415) | GCC185, RANBP2L4, REN53 | 612711 |
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: 8992 | ATPase H+ transporting V0 subunit e1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (172983771..173035445) | ATP6H, ATP6V0E, M9.2, Vma21, Vma21p | 603931 |
ID: 6138 | ribosomal protein L15 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (23916545..23924631) | DBA12, EC45, L15, RPL10, RPLY10, RPYL10, eL15 | 604174 |
ID: 80723 | solute carrier family 35 member G2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (136819126..136855888) | TMEM22 | 617812 |
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: 28969 | basic leucine zipper and W2 domains 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (16646181..16706517) | 5MP1, HSPC028, MST017, MSTP017 | 619275 |
ID: 9512 | peptidase, mitochondrial processing subunit beta [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (103297435..103347542) | Beta-MPP, MAS1, MPP11, MPPB, MPPP52, P-52 | 603131 |
ID: 54439 | RNA binding motif protein 27 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (146203605..146289223) | ARRS1, Psc1, ZC3H18, ZC3H20 | 620082 |
ID: 29097 | cornichon family member 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (224356803..224379452) | CNIH-4, CNIH2, HSPC163 | 617483 |
ID: 55183 | replication timing regulatory factor 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (151409902..151534435) | | 608952 |